Canonical Allele Identifier: CA867157055
Gene: PSAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1400180451
gnomAD v3: 9-78329939-T-C
gnomAD v4: 9-78329939-T-C
MyVariant Identifiers: chr9:g.80944855T>C (hg19) chr9:g.78329939T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329939T>C , CM000671.2:g.78329939T>C GRCh38
NC_000009.11:g.80944855T>C , CM000671.1:g.80944855T>C GRCh37
NC_000009.10:g.80134675T>C NCBI36
NG_012165.1:g.37797T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*853T>C MANE Select ENSP00000365773.3:n.*853T>C
ENST00000376588.3:c.*853T>C ENSP00000365773.3:n.*853T>C
NM_021154.4:c.*853T>C NP_066977.1:n.*853T>C
NM_058179.3:c.*853T>C NP_478059.1:n.*853T>C
NM_058179.4:c.*853T>C MANE Select NP_478059.1:n.*853T>C
NM_021154.5:c.*853T>C NP_066977.1:n.*853T>C
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