Canonical Allele Identifier: CA2652478034
Gene: SNTA1 HGNC NCBI

Linked Data

gnomAD v4: 20-33438823-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438823T>G , CM000682.2:g.33438823T>G GRCh38
NC_000020.10:g.32026629T>G , CM000682.1:g.32026629T>G GRCh37
NC_000020.9:g.31490290T>G NCBI36
NG_011622.1:g.10070A>C , LRG_332:g.10070A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.3:c.496+18A>C MANE Select ENSP00000217381.2:n.496+18A>C
ENST00000217381.2:c.496+18A>C ENSP00000217381.2:n.496+18A>C
NM_003098.2:c.496+18A>C , LRG_332t1:c.496+18A>C NP_003089.1:n.496+18A>C
XM_005260517.1:c.496+18A>C XP_005260574.1:n.496+18A>C
XM_011529007.1:c.496+18A>C XP_011527309.1:n.496+18A>C
XM_011529008.1:c.496+18A>C XP_011527310.1:n.496+18A>C
XR_936612.1:n.729+18A>C
XM_024451971.1:c.169+18A>C XP_024307739.1:n.169+18A>C
NM_003098.3:c.496+18A>C MANE Select NP_003089.1:n.496+18A>C
Search 100 bp 5'
Search 100 bp 3'