Canonical Allele Identifier: CA2523885922
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1990643475
gnomAD v4: 20-33443780-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443780T>G , CM000682.2:g.33443780T>G GRCh38
NC_000020.10:g.32031586T>G , CM000682.1:g.32031586T>G GRCh37
NC_000020.9:g.31495247T>G NCBI36
NG_011622.1:g.5113A>C , LRG_332:g.5113A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.2:c.-160A>C ENSP00000217381.2:n.-160A>C
NM_003098.2:c.-160A>C , LRG_332t1:c.-160A>C NP_003089.1:n.-160A>C
XM_005260517.1:c.-160A>C XP_005260574.1:n.-160A>C
XM_011529007.1:c.-160A>C XP_011527309.1:n.-160A>C
XM_011529008.1:c.-160A>C XP_011527310.1:n.-160A>C
XR_936612.1:n.74A>C
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