Canonical Allele Identifier: CA1264999460
Gene:

Linked Data

dbSNP Id: rs1450494088

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.81645847G>T , CM000664.2:g.81645847G>T GRCh38
NC_000002.11:g.81872971G>T , CM000664.1:g.81872971G>T GRCh37
NC_000002.10:g.81726482G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940294.1:n.563+66238G>T
XR_940295.1:n.485+97100G>T
XR_001739571.1:n.485+97100G>T