Canonical Allele Identifier: CA1573933640
Gene:

Linked Data

dbSNP Id: rs1780061956

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660886T>G , CM000667.2:g.113660886T>G GRCh38
NC_000005.9:g.112996583T>G , CM000667.1:g.112996583T>G GRCh37
NC_000005.8:g.113024482T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27522T>G