Canonical Allele Identifier: CA1610684915
Gene:

Linked Data

dbSNP Id: rs1766142424

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943600G>A , CM000668.2:g.11943600G>A GRCh38
NC_000006.11:g.11943833G>A , CM000668.1:g.11943833G>A GRCh37
NC_000006.10:g.12051819G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7935G>A