Canonical Allele Identifier: CA867157009
Gene: PSAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1477576296
MyVariant Identifiers: chr9:g.80944782A>G (hg19) chr9:g.78329866A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78329866A>G , CM000671.2:g.78329866A>G GRCh38
NC_000009.11:g.80944782A>G , CM000671.1:g.80944782A>G GRCh37
NC_000009.10:g.80134602A>G NCBI36
NG_012165.1:g.37724A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.*780A>G MANE Select ENSP00000365773.3:n.*780A>G
ENST00000376588.3:c.*780A>G ENSP00000365773.3:n.*780A>G
NM_021154.4:c.*780A>G NP_066977.1:n.*780A>G
NM_058179.3:c.*780A>G NP_478059.1:n.*780A>G
NM_058179.4:c.*780A>G MANE Select NP_478059.1:n.*780A>G
NM_021154.5:c.*780A>G NP_066977.1:n.*780A>G
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