Canonical Allele Identifier: CA2652478577
Gene: SNTA1 HGNC NCBI

Linked Data

gnomAD v4: 20-33443708-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443708C>G , CM000682.2:g.33443708C>G GRCh38
NC_000020.10:g.32031514C>G , CM000682.1:g.32031514C>G GRCh37
NC_000020.9:g.31495175C>G NCBI36
NG_011622.1:g.5185G>C , LRG_332:g.5185G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.-88G>C MANE Select ENSP00000217381.2:n.-88G>C
ENST00000217381.2:c.-88G>C ENSP00000217381.2:n.-88G>C
NM_003098.2:c.-88G>C , LRG_332t1:c.-88G>C NP_003089.1:n.-88G>C
XM_005260517.1:c.-88G>C XP_005260574.1:n.-88G>C
XM_011529007.1:c.-88G>C XP_011527309.1:n.-88G>C
XM_011529008.1:c.-88G>C XP_011527310.1:n.-88G>C
XR_936612.1:n.146G>C
NM_003098.3:c.-88G>C MANE Select NP_003089.1:n.-88G>C
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