Canonical Allele Identifier: CA2577372710
Gene: SNTA1 HGNC NCBI

Linked Data

gnomAD v4: 20-33443712-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443712G>A , CM000682.2:g.33443712G>A GRCh38
NC_000020.10:g.32031518G>A , CM000682.1:g.32031518G>A GRCh37
NC_000020.9:g.31495179G>A NCBI36
NG_011622.1:g.5181C>T , LRG_332:g.5181C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.3:c.-92C>T MANE Select ENSP00000217381.2:n.-92C>T
ENST00000217381.2:c.-92C>T ENSP00000217381.2:n.-92C>T
NM_003098.2:c.-92C>T , LRG_332t1:c.-92C>T NP_003089.1:n.-92C>T
XM_005260517.1:c.-92C>T XP_005260574.1:n.-92C>T
XM_011529007.1:c.-92C>T XP_011527309.1:n.-92C>T
XM_011529008.1:c.-92C>T XP_011527310.1:n.-92C>T
XR_936612.1:n.142C>T
NM_003098.3:c.-92C>T MANE Select NP_003089.1:n.-92C>T
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