Canonical Allele Identifier: CA1573933650
Gene:

Linked Data

dbSNP Id: rs1490067046

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660895C>G , CM000667.2:g.113660895C>G GRCh38
NC_000005.9:g.112996592C>G , CM000667.1:g.112996592C>G GRCh37
NC_000005.8:g.113024491C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27531C>G