Canonical Allele Identifier: CA588653594
Gene: PSAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1490618598
gnomAD v2: 9-80944902-A-T
gnomAD v3: 9-78329986-A-T
gnomAD v4: 9-78329986-A-T
MyVariant Identifiers: chr9:g.80944902A>T (hg19) chr9:g.78329986A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329986A>T , CM000671.2:g.78329986A>T GRCh38
NC_000009.11:g.80944902A>T , CM000671.1:g.80944902A>T GRCh37
NC_000009.10:g.80134722A>T NCBI36
NG_012165.1:g.37844A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*900A>T MANE Select ENSP00000365773.3:n.*900A>T
ENST00000376588.3:c.*900A>T ENSP00000365773.3:n.*900A>T
NM_021154.4:c.*900A>T NP_066977.1:n.*900A>T
NM_058179.3:c.*900A>T NP_478059.1:n.*900A>T
NM_058179.4:c.*900A>T MANE Select NP_478059.1:n.*900A>T
NM_021154.5:c.*900A>T NP_066977.1:n.*900A>T
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