Canonical Allele Identifier: CA373871573
Gene: PSAT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.80915564G>T (hg19) chr9:g.78300648G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.78300648G>T , CM000671.2:g.78300648G>T GRCh38
NC_000009.11:g.80915564G>T , CM000671.1:g.80915564G>T GRCh37
NC_000009.10:g.80105384G>T NCBI36
NG_012165.1:g.8506G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376588.4:c.107G>T MANE Select ENSP00000365773.3:p.Gly36Val
ENST00000347159.6:c.107G>T ENSP00000317606.2:p.Gly36Val
ENST00000376588.3:c.107G>T ENSP00000365773.3:p.Gly36Val
NM_021154.4:c.107G>T NP_066977.1:p.Gly36Val
NM_058179.3:c.107G>T NP_478059.1:p.Gly36Val
NM_058179.4:c.107G>T MANE Select NP_478059.1:p.Gly36Val
NM_021154.5:c.107G>T NP_066977.1:p.Gly36Val
Search 100 bp 5'
Search 100 bp 3'