Canonical Allele Identifier: CA666858066
Gene:

Linked Data

dbSNP Id: rs1319813543

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812902C>T , CM000672.2:g.57812902C>T GRCh38
NC_000010.10:g.59572662C>T , CM000672.1:g.59572662C>T GRCh37
NC_000010.9:g.59242668C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34390G>A
XR_001747454.1:n.85+34390G>A