Canonical Allele Identifier: CA1649534210
Gene:

Linked Data

dbSNP Id: rs1773158616

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102367G>A , CM000668.2:g.98102367G>A GRCh38
NC_000006.11:g.98550243G>A , CM000668.1:g.98550243G>A GRCh37
NC_000006.10:g.98656964G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.456+3097G>A
XR_942809.1:n.456+3097G>A