Canonical Allele Identifier: CA3197755750
Community Standard Title: NM_000277.3(PAH):c.660T= (p.His220=)
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855182A= , CM000674.2:g.102855182A= GRCh38
NC_000012.11:g.103248960A= , CM000674.1:g.103248960A= GRCh37
NC_000012.10:g.101773090A= NCBI36
NG_008690.1:g.67421T=
NG_008690.2:g.108229T=

Transcript Alleles

HGVS Amino-acid Change
NM_000277.3:c.660T= MANE Select NP_000268.1:p.His220=
ENST00000553106.6:c.660T= MANE Select ENSP00000448059.1:p.His220=
NM_000277.1:c.660T= NP_000268.1:p.His220=
NM_000277.2:c.660T= NP_000268.1:p.His220=
NM_001354304.1:c.660T= NP_001341233.1:p.His220=
NM_001354304.2:c.660T= NP_001341233.1:p.His220=
ENST00000307000.7:c.645T= ENSP00000303500.2:p.His215=
ENST00000549111.5:n.756T=
ENST00000553106.5:c.660T= ENSP00000448059.1:p.His220=
XM_011538422.1:c.660T= XP_011536724.1:p.His220=
XM_017019370.2:c.660T= XP_016874859.1:p.His220=
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