Canonical Allele Identifier: CA2059443819
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1875137291

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102851279T>C , CM000674.2:g.102851279T>C GRCh38
NC_000012.11:g.103245057T>C , CM000674.1:g.103245057T>C GRCh37
NC_000012.10:g.101769187T>C NCBI36
NG_008690.1:g.71324A>G
NG_008690.2:g.112132A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.912+408A>G MANE Select ENSP00000448059.1:n.912+408A>G
ENST00000307000.7:c.897+408A>G ENSP00000303500.2:n.897+408A>G
ENST00000549247.6:n.671+408A>G
ENST00000551114.2:n.574+408A>G
ENST00000553106.5:c.912+408A>G ENSP00000448059.1:n.912+408A>G
ENST00000635477.1:c.73+408A>G
NM_000277.1:c.912+408A>G NP_000268.1:n.912+408A>G
XM_011538422.1:c.912+408A>G XP_011536724.1:n.912+408A>G
NM_000277.2:c.912+408A>G NP_000268.1:n.912+408A>G
NM_001354304.1:c.912+408A>G NP_001341233.1:n.912+408A>G
NM_000277.3:c.912+408A>G MANE Select NP_000268.1:n.912+408A>G
NM_001354304.2:c.912+408A>G NP_001341233.1:n.912+408A>G