Canonical Allele Identifier: CA1775343156
Gene:

Linked Data

dbSNP Id: rs199500724

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808361G>C , CM000670.2:g.33808361G>C GRCh38
NC_000008.10:g.33665879G>C , CM000670.1:g.33665879G>C GRCh37
NC_000008.9:g.33785421G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949659.1:n.240+11925G>C
XR_002956701.1:n.240+11925G>C