Canonical Allele Identifier: CA64121840
Gene:

Linked Data

dbSNP Id: rs987561580

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767686A>C , CM000664.2:g.198767686A>C GRCh38
NC_000002.11:g.199632410A>C , CM000664.1:g.199632410A>C GRCh37
NC_000002.10:g.199340655A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923758.1:n.72+4573T>G
XR_923759.1:n.72+4573T>G
XR_923760.1:n.72+4573T>G
XR_923759.2:n.72+4573T>G
XR_923760.2:n.72+4573T>G