Canonical Allele Identifier: CA1205765984
Gene:

Linked Data

dbSNP Id: rs1648344093

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649359G>A , CM000663.2:g.168649359G>A GRCh38
NC_000001.10:g.168618597G>A , CM000663.1:g.168618597G>A GRCh37
NC_000001.9:g.166885221G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8084C>T
XR_922259.2:n.332-8084C>T