Canonical Allele Identifier: CA2360755107
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs898788313
gnomAD v4: 20-33443713-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443713G>T , CM000682.2:g.33443713G>T GRCh38
NC_000020.10:g.32031519G>T , CM000682.1:g.32031519G>T GRCh37
NC_000020.9:g.31495180G>T NCBI36
NG_011622.1:g.5180C>A , LRG_332:g.5180C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.-93C>A MANE Select ENSP00000217381.2:n.-93C>A
ENST00000217381.2:c.-93C>A ENSP00000217381.2:n.-93C>A
NM_003098.2:c.-93C>A , LRG_332t1:c.-93C>A NP_003089.1:n.-93C>A
XM_005260517.1:c.-93C>A XP_005260574.1:n.-93C>A
XM_011529007.1:c.-93C>A XP_011527309.1:n.-93C>A
XM_011529008.1:c.-93C>A XP_011527310.1:n.-93C>A
XR_936612.1:n.141C>A
NM_003098.3:c.-93C>A MANE Select NP_003089.1:n.-93C>A
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