Canonical Allele Identifier: CA2698684590
Gene:

Linked Data

dbSNP Id: rs2103349953

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458190C>A , CM000664.2:g.16458190C>A GRCh38
NC_000002.11:g.16639458C>A , CM000664.1:g.16639458C>A GRCh37
NC_000002.10:g.16502939C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939752.1:n.396-3096G>T