Canonical Allele Identifier: CA994936001
Gene:

Linked Data

dbSNP Id: rs2011164404

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544586A>C , CM000681.2:g.28544586A>C GRCh38
NC_000019.9:g.29035493A>C , CM000681.1:g.29035493A>C GRCh37
NC_000019.8:g.33727333A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77806T>G
XR_243979.1:n.110-51563T>G