Canonical Allele Identifier: CA539151228
Gene:

Linked Data

dbSNP Id: rs775314021

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203934626T>A , CM000664.2:g.203934626T>A GRCh38
NC_000002.11:g.204799349T>A , CM000664.1:g.204799349T>A GRCh37
NC_000002.10:g.204507594T>A NCBI36
NG_011586.1:g.2847T>A , LRG_65:g.2847T>A

Transcript Alleles

HGVS Amino-acid change
XR_427213.2:n.460+1482A>T
XR_001739861.1:n.1642A>T
XR_427213.3:n.474+1482A>T