Canonical Allele Identifier: CA2330336292
Gene:

Linked Data

dbSNP Id: rs2011164836

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544665A>G , CM000681.2:g.28544665A>G GRCh38
NC_000019.9:g.29035572A>G , CM000681.1:g.29035572A>G GRCh37
NC_000019.8:g.33727412A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77885T>C
XR_243979.1:n.110-51642T>C