Canonical Allele Identifier: CA666858052
Gene:

Linked Data

dbSNP Id: rs1317445243

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812868A>T , CM000672.2:g.57812868A>T GRCh38
NC_000010.10:g.59572628A>T , CM000672.1:g.59572628A>T GRCh37
NC_000010.9:g.59242634A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34424T>A
XR_001747454.1:n.85+34424T>A