Canonical Allele Identifier: CA2330336271
Gene:

Linked Data

dbSNP Id: rs2011164646

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544632A>G , CM000681.2:g.28544632A>G GRCh38
NC_000019.9:g.29035539A>G , CM000681.1:g.29035539A>G GRCh37
NC_000019.8:g.33727379A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110759.1:n.657-77852T>C
XR_243979.1:n.110-51609T>C