Canonical Allele Identifier: CA2330336347
Gene:

Linked Data

dbSNP Id: rs1599600975

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544786A>G , CM000681.2:g.28544786A>G GRCh38
NC_000019.9:g.29035693A>G , CM000681.1:g.29035693A>G GRCh37
NC_000019.8:g.33727533A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110759.1:n.657-78006T>C
XR_243979.1:n.110-51763T>C