Canonical Allele Identifier: CA2719899104

Gene: PSAT1

Linked Data

• dbSNP Id: rs2118720978

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78329925A>G , CM000671.2:g.78329925A>G	GRCh38
NC_000009.11:g.80944841A>G , CM000671.1:g.80944841A>G	GRCh37
NC_000009.10:g.80134661A>G	NCBI36
NG_012165.1:g.37783A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376588.4:c.*839A>G MANE Select	ENSP00000365773.3:n.*839A>G
ENST00000376588.3:c.*839A>G	ENSP00000365773.3:n.*839A>G
NM_021154.4:c.*839A>G	NP_066977.1:n.*839A>G
NM_058179.3:c.*839A>G	NP_478059.1:n.*839A>G
NM_058179.4:c.*839A>G MANE Select	NP_478059.1:n.*839A>G
NM_021154.5:c.*839A>G	NP_066977.1:n.*839A>G