Canonical Allele Identifier: CA2047190478
Gene:

Linked Data

dbSNP Id: rs1870342072

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004902C>T , CM000674.2:g.76004902C>T GRCh38
NC_000012.11:g.76398682C>T , CM000674.1:g.76398682C>T GRCh37
NC_000012.10:g.74684949C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945110.1:n.311+1287G>A
XR_001749218.2:n.402+1287G>A
XR_945110.3:n.402+1287G>A