Canonical Allele Identifier: CA1675056618
Gene:

Linked Data

dbSNP Id: rs9397906

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156171540G>T , CM000668.2:g.156171540G>T GRCh38
NC_000006.11:g.156492674G>T , CM000668.1:g.156492674G>T GRCh37
NC_000006.10:g.156534366G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943146.1:n.193-3046C>A
XR_001744423.1:n.247-3046C>A