Canonical Allele Identifier: CA1205765991
Gene:

Linked Data

dbSNP Id: rs1648344418

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649372C>T , CM000663.2:g.168649372C>T GRCh38
NC_000001.10:g.168618610C>T , CM000663.1:g.168618610C>T GRCh37
NC_000001.9:g.166885234C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8097G>A
XR_922259.2:n.332-8097G>A