Canonical Allele Identifier: CA1858359255
Gene:

Linked Data

dbSNP Id: rs2076503416

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.79730996G>A , CM000671.2:g.79730996G>A GRCh38
NC_000009.11:g.82345911G>A , CM000671.1:g.82345911G>A GRCh37
NC_000009.10:g.81535731G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929980.1:n.1019+684G>A