Canonical Allele Identifier: CA1610684884
Gene:

Linked Data

dbSNP Id: rs1766141914

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943554A>G , CM000668.2:g.11943554A>G GRCh38
NC_000006.11:g.11943787A>G , CM000668.1:g.11943787A>G GRCh37
NC_000006.10:g.12051773A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7981A>G