Canonical Allele Identifier: CA1468682078
Gene:

Linked Data

dbSNP Id: rs1721060342

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74553999T>G , CM000666.2:g.74553999T>G GRCh38
NC_000004.11:g.75419716T>G , CM000666.1:g.75419716T>G GRCh37
NC_000004.10:g.75638580T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741513.1:n.167-1167A>C