Canonical Allele Identifier: CA229591
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102709
ClinVar RCV Id: RCV000088957
dbSNP Id: rs62517171
MyVariant Identifiers: chr12:g.103260320G>C (hg19) chr12:g.102866542G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102866542G>C , CM000674.2:g.102866542G>C GRCh38
NC_000012.11:g.103260320G>C , CM000674.1:g.103260320G>C GRCh37
NC_000012.10:g.101784450G>C NCBI36
NG_008690.1:g.56061C>G
NG_008690.2:g.96869C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.509+54C>G MANE Select ENSP00000448059.1:n.509+54C>G
ENST00000307000.7:c.494+54C>G ENSP00000303500.2:n.494+54C>G
ENST00000549111.5:n.605+54C>G
ENST00000551988.5:n.530+10920C>G
ENST00000553106.5:c.509+54C>G ENSP00000448059.1:n.509+54C>G
NM_000277.1:c.509+54C>G NP_000268.1:n.509+54C>G
XM_011538422.1:c.509+54C>G XP_011536724.1:n.509+54C>G
NM_000277.2:c.509+54C>G NP_000268.1:n.509+54C>G
NM_001354304.1:c.509+54C>G NP_001341233.1:n.509+54C>G
XM_017019370.2:c.509+54C>G XP_016874859.1:n.509+54C>G
NM_000277.3:c.509+54C>G MANE Select NP_000268.1:n.509+54C>G
NM_001354304.2:c.509+54C>G NP_001341233.1:n.509+54C>G
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