Canonical Allele Identifier: CA2733637140
Gene:

Linked Data

dbSNP Id: rs2153018000

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29376269A>G , CM000679.2:g.29376269A>G GRCh38
NC_000017.10:g.27703287A>G , CM000679.1:g.27703287A>G GRCh37
NC_000017.9:g.24727413A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011525588.1:c.1008-5964T>C XP_011523890.1:n.1008-5964T>C