Canonical Allele Identifier: CA1322177722
Gene:

Linked Data

dbSNP Id: rs1689615942

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203934613A>T , CM000664.2:g.203934613A>T GRCh38
NC_000002.11:g.204799336A>T , CM000664.1:g.204799336A>T GRCh37
NC_000002.10:g.204507581A>T NCBI36
NG_011586.1:g.2834A>T , LRG_65:g.2834A>T

Transcript Alleles

HGVS Amino-acid change
XR_427213.2:n.460+1495T>A
XR_001739861.1:n.1655T>A
XR_427213.3:n.474+1495T>A