Canonical Allele Identifier: CA2652476848
Gene: SNTA1 HGNC NCBI

Linked Data

gnomAD v4: 20-33408447-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33408447A>G , CM000682.2:g.33408447A>G GRCh38
NC_000020.10:g.31996253A>G , CM000682.1:g.31996253A>G GRCh37
NC_000020.9:g.31459914A>G NCBI36
NG_011622.1:g.40446T>C , LRG_332:g.40446T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000217381.3:c.*60T>C MANE Select ENSP00000217381.2:n.*60T>C
ENST00000217381.2:c.*60T>C ENSP00000217381.2:n.*60T>C
NM_003098.2:c.*60T>C , LRG_332t1:c.*60T>C NP_003089.1:n.*60T>C
XM_005260517.1:c.*60T>C XP_005260574.1:n.*60T>C
XM_011529007.1:c.*119T>C XP_011527309.1:n.*119T>C
XM_011529008.1:c.*119T>C XP_011527310.1:n.*119T>C
XR_936612.1:n.1614T>C
XM_024451971.1:c.*60T>C XP_024307739.1:n.*60T>C
NM_003098.3:c.*60T>C MANE Select NP_003089.1:n.*60T>C
Search 100 bp 5'
Search 100 bp 3'