Canonical Allele Identifier: CA1228390019
Gene:

Linked Data

dbSNP Id: rs2069084

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.234849241G>C , CM000663.2:g.234849241G>C GRCh38
NC_000001.10:g.234984988G>C , CM000663.1:g.234984988G>C GRCh37
NC_000001.9:g.233051611G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738533.1:n.2809+21361C>G
XR_001738534.1:n.1268+21361C>G