Canonical Allele Identifier: CA1675056619
Gene:

Linked Data

dbSNP Id: rs9397906

Genomic Alleles

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

Transcript Alleles

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