Canonical Allele Identifier: CA1610684975
Gene:

Linked Data

dbSNP Id: rs1581439198

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943701G>A , CM000668.2:g.11943701G>A GRCh38
NC_000006.11:g.11943934G>A , CM000668.1:g.11943934G>A GRCh37
NC_000006.10:g.12051920G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7834G>A