Canonical Allele Identifier: CA373872011
Gene: PSAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78304751T>C , CM000671.2:g.78304751T>C GRCh38
NC_000009.11:g.80919667T>C , CM000671.1:g.80919667T>C GRCh37
NC_000009.10:g.80109487T>C NCBI36
NG_012165.1:g.12609T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.208T>C MANE Select ENSP00000365773.3:p.Tyr70His
ENST00000347159.6:c.208T>C ENSP00000317606.2:p.Tyr70His
ENST00000376588.3:c.208T>C ENSP00000365773.3:p.Tyr70His
NM_021154.4:c.208T>C NP_066977.1:p.Tyr70His
NM_058179.3:c.208T>C NP_478059.1:p.Tyr70His
NM_058179.4:c.208T>C MANE Select NP_478059.1:p.Tyr70His
NM_021154.5:c.208T>C NP_066977.1:p.Tyr70His