Canonical Allele Identifier: CA481331542
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1592953026
MyVariant Identifiers: chr12:g.103246685G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852907G>C , CM000674.2:g.102852907G>C GRCh38
NC_000012.11:g.103246685G>C , CM000674.1:g.103246685G>C GRCh37
NC_000012.10:g.101770815G>C NCBI36
NG_008690.1:g.69696C>G
NG_008690.2:g.110504C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.750C>G MANE Select ENSP00000448059.1:p.Ser250=
ENST00000307000.7:c.735C>G ENSP00000303500.2:p.Ser245=
ENST00000549247.6:n.509C>G
ENST00000553106.5:c.750C>G ENSP00000448059.1:p.Ser250=
NM_000277.1:c.750C>G NP_000268.1:p.Ser250=
XM_011538422.1:c.750C>G XP_011536724.1:p.Ser250=
NM_000277.2:c.750C>G NP_000268.1:p.Ser250=
NM_001354304.1:c.750C>G NP_001341233.1:p.Ser250=
NM_000277.3:c.750C>G MANE Select NP_000268.1:p.Ser250=
NM_001354304.2:c.750C>G NP_001341233.1:p.Ser250=