Canonical Allele Identifier: CA692339928
Gene:

Linked Data

dbSNP Id: rs1458133785

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069309C>T , CM000674.2:g.80069309C>T GRCh38
NC_000012.11:g.80463089C>T , CM000674.1:g.80463089C>T GRCh37
NC_000012.10:g.78987220C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945140.1:n.456+8127C>T
XR_945141.1:n.1758+8127C>T