Canonical Allele Identifier: CA2360755157
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1600868856
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443785T>G , CM000682.2:g.33443785T>G GRCh38
NC_000020.10:g.32031591T>G , CM000682.1:g.32031591T>G GRCh37
NC_000020.9:g.31495252T>G NCBI36
NG_011622.1:g.5108A>C , LRG_332:g.5108A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.2:c.-165A>C ENSP00000217381.2:n.-165A>C
NM_003098.2:c.-165A>C , LRG_332t1:c.-165A>C NP_003089.1:n.-165A>C
XM_005260517.1:c.-165A>C XP_005260574.1:n.-165A>C
XM_011529007.1:c.-165A>C XP_011527309.1:n.-165A>C
XM_011529008.1:c.-165A>C XP_011527310.1:n.-165A>C
XR_936612.1:n.69A>C
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