Canonical Allele Identifier: CA2254736359
Gene:

Linked Data

dbSNP Id: rs1598455560

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29376286T>C , CM000679.2:g.29376286T>C GRCh38
NC_000017.10:g.27703304T>C , CM000679.1:g.27703304T>C GRCh37
NC_000017.9:g.24727430T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011525588.1:c.1008-5981A>G XP_011523890.1:n.1008-5981A>G