Canonical Allele Identifier: CA2047190512
Gene:

Linked Data

dbSNP Id: rs1870343888

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004977G>A , CM000674.2:g.76004977G>A GRCh38
NC_000012.11:g.76398757G>A , CM000674.1:g.76398757G>A GRCh37
NC_000012.10:g.74685024G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945110.1:n.311+1212C>T
XR_001749218.2:n.402+1212C>T
XR_945110.3:n.402+1212C>T