Canonical Allele Identifier: CA2491383649
Gene:

Linked Data

dbSNP Id: rs1664552997

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458276G>A , CM000664.2:g.16458276G>A GRCh38
NC_000002.11:g.16639544G>A , CM000664.1:g.16639544G>A GRCh37
NC_000002.10:g.16503025G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939752.1:n.396-3182C>T