Canonical Allele Identifier: CA1605276857
Gene:

Linked Data

dbSNP Id: rs1762568958

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465903G>A , CM000668.2:g.465903G>A GRCh38
NC_000006.11:g.465903G>A , CM000668.1:g.465903G>A GRCh37
NC_000006.10:g.410903G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12178G>A
XR_926365.1:n.2548+12178G>A
XR_001743914.1:n.482-9305G>A