Canonical Allele Identifier: CA2360755103
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1990640765
gnomAD v4: 20-33443711-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443711G>C , CM000682.2:g.33443711G>C GRCh38
NC_000020.10:g.32031517G>C , CM000682.1:g.32031517G>C GRCh37
NC_000020.9:g.31495178G>C NCBI36
NG_011622.1:g.5182C>G , LRG_332:g.5182C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.3:c.-91C>G MANE Select ENSP00000217381.2:n.-91C>G
ENST00000217381.2:c.-91C>G ENSP00000217381.2:n.-91C>G
NM_003098.2:c.-91C>G , LRG_332t1:c.-91C>G NP_003089.1:n.-91C>G
XM_005260517.1:c.-91C>G XP_005260574.1:n.-91C>G
XM_011529007.1:c.-91C>G XP_011527309.1:n.-91C>G
XM_011529008.1:c.-91C>G XP_011527310.1:n.-91C>G
XR_936612.1:n.143C>G
NM_003098.3:c.-91C>G MANE Select NP_003089.1:n.-91C>G
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