Canonical Allele Identifier: CA229793
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102855
ClinVar RCV Id: RCV000089116 RCV000670910
dbSNP Id: rs62508715
MyVariant Identifiers: chr12:g.103246611G>A (hg19) chr12:g.102852833G>A (hg38)
ERepo: CA229793/MONDO:0009861/006
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852833G>A , CM000674.2:g.102852833G>A GRCh38
NC_000012.11:g.103246611G>A , CM000674.1:g.103246611G>A GRCh37
NC_000012.10:g.101770741G>A NCBI36
NG_008690.1:g.69770C>T
NG_008690.2:g.110578C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.824C>T MANE Select ENSP00000448059.1:p.Pro275Leu
ENST00000307000.7:c.809C>T ENSP00000303500.2:p.Pro270Leu
ENST00000549247.6:n.583C>T
ENST00000553106.5:c.824C>T ENSP00000448059.1:p.Pro275Leu
NM_000277.1:c.824C>T NP_000268.1:p.Pro275Leu
XM_011538422.1:c.824C>T XP_011536724.1:p.Pro275Leu
NM_000277.2:c.824C>T NP_000268.1:p.Pro275Leu
NM_001354304.1:c.824C>T NP_001341233.1:p.Pro275Leu
NM_000277.3:c.824C>T MANE Select NP_000268.1:p.Pro275Leu
NM_001354304.2:c.824C>T NP_001341233.1:p.Pro275Leu
Search 100 bp 5'
Search 100 bp 3'