Canonical Allele Identifier: CA2345844038
Gene:

Linked Data

dbSNP Id: rs156339

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1875546A>C , CM000682.2:g.1875546A>C GRCh38
NC_000020.10:g.1856192A>C , CM000682.1:g.1856192A>C GRCh37
NC_000020.9:g.1804192A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754467.1:n.433-7453T>G