Canonical Allele Identifier: CA289219336
Gene:

Linked Data

dbSNP Id: rs1003143152

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29376348A>G , CM000679.2:g.29376348A>G GRCh38
NC_000017.10:g.27703366A>G , CM000679.1:g.27703366A>G GRCh37
NC_000017.9:g.24727492A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011525588.1:c.1008-6043T>C XP_011523890.1:n.1008-6043T>C