Canonical Allele Identifier: CA386295862
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1875247427

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852950G>C , CM000674.2:g.102852950G>C GRCh38
NC_000012.11:g.103246728G>C , CM000674.1:g.103246728G>C GRCh37
NC_000012.10:g.101770858G>C NCBI36
NG_008690.1:g.69653C>G
NG_008690.2:g.110461C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.707C>G MANE Select ENSP00000448059.1:p.Thr236Ser
ENST00000307000.7:c.692C>G ENSP00000303500.2:p.Thr231Ser
ENST00000549247.6:n.466C>G
ENST00000553106.5:c.707C>G ENSP00000448059.1:p.Thr236Ser
NM_000277.1:c.707C>G NP_000268.1:p.Thr236Ser
XM_011538422.1:c.707C>G XP_011536724.1:p.Thr236Ser
NM_000277.2:c.707C>G NP_000268.1:p.Thr236Ser
NM_001354304.1:c.707C>G NP_001341233.1:p.Thr236Ser
NM_000277.3:c.707C>G MANE Select NP_000268.1:p.Thr236Ser
NM_001354304.2:c.707C>G NP_001341233.1:p.Thr236Ser