Canonical Allele Identifier: CA2047190473
Gene:

Linked Data

dbSNP Id: rs1870341942

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004895G>C , CM000674.2:g.76004895G>C GRCh38
NC_000012.11:g.76398675G>C , CM000674.1:g.76398675G>C GRCh37
NC_000012.10:g.74684942G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945110.1:n.311+1294C>G
XR_001749218.2:n.402+1294C>G
XR_945110.3:n.402+1294C>G