Canonical Allele Identifier: CA2736316876
Gene:

Linked Data

dbSNP Id: rs2122868611

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1875499C>T , CM000682.2:g.1875499C>T GRCh38
NC_000020.10:g.1856145C>T , CM000682.1:g.1856145C>T GRCh37
NC_000020.9:g.1804145C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754467.1:n.433-7406G>A