Canonical Allele Identifier: CA2254741080
Gene:

Linked Data

dbSNP Id: rs8076739

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29387569C>G , CM000679.2:g.29387569C>G GRCh38
NC_000017.10:g.27714587C>G , CM000679.1:g.27714587C>G GRCh37
NC_000017.9:g.24738713C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011525588.1:c.1007+2368G>C XP_011523890.1:n.1007+2368G>C