Canonical Allele Identifier: CA2652478582
Gene: SNTA1 HGNC NCBI

Linked Data

gnomAD v4: 20-33443713-G-C
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.3:c.-93C>G MANE Select ENSP00000217381.2:n.-93C>G
ENST00000217381.2:c.-93C>G ENSP00000217381.2:n.-93C>G
NM_003098.2:c.-93C>G , LRG_332t1:c.-93C>G NP_003089.1:n.-93C>G
XM_005260517.1:c.-93C>G XP_005260574.1:n.-93C>G
XM_011529007.1:c.-93C>G XP_011527309.1:n.-93C>G
XM_011529008.1:c.-93C>G XP_011527310.1:n.-93C>G
XR_936612.1:n.141C>G
NM_003098.3:c.-93C>G MANE Select NP_003089.1:n.-93C>G
Search 100 bp 5'
Search 100 bp 3'