Canonical Allele Identifier: CA2345844005
Gene:

Linked Data

dbSNP Id: rs1983027381

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1875501C>T , CM000682.2:g.1875501C>T GRCh38
NC_000020.10:g.1856147C>T , CM000682.1:g.1856147C>T GRCh37
NC_000020.9:g.1804147C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754467.1:n.433-7408G>A