Canonical Allele Identifier: CA632202284
Gene:

Linked Data

dbSNP Id: rs1402806670

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544571T>C , CM000681.2:g.28544571T>C GRCh38
NC_000019.9:g.29035478T>C , CM000681.1:g.29035478T>C GRCh37
NC_000019.8:g.33727318T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110759.1:n.657-77791A>G
XR_243979.1:n.110-51548A>G