Canonical Allele Identifier: CA1286885948
Gene:

Linked Data

dbSNP Id: rs1688786255

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431655C>T , CM000664.2:g.127431655C>T GRCh38
NC_000002.11:g.128189231C>T , CM000664.1:g.128189231C>T GRCh37
NC_000002.10:g.127905701C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+12G>A
XR_001739705.1:n.3607-3391G>A
XR_923313.2:n.4042+12G>A