Canonical Allele Identifier: CA602555876
Gene:

Linked Data

dbSNP Id: rs1305320498

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128455618G>T , CM000673.2:g.128455618G>T GRCh38
NC_000011.9:g.128325513G>T , CM000673.1:g.128325513G>T GRCh37
NC_000011.8:g.127830723G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948164.1:n.4338G>T
XR_948165.1:n.3467+871G>T