Canonical Allele Identifier: CA756214949
Gene:

Linked Data

dbSNP Id: rs1305071730

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883974G>T , CM000664.2:g.122883974G>T GRCh38
NC_000002.11:g.123641550G>T , CM000664.1:g.123641550G>T GRCh37
NC_000002.10:g.123358020G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-968G>T
XR_001739692.1:n.1451-968G>T
XR_923292.2:n.1358-968G>T