Canonical Allele Identifier: CA1610684934
Gene:

Linked Data

dbSNP Id: rs1766142840

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943639A>G , CM000668.2:g.11943639A>G GRCh38
NC_000006.11:g.11943872A>G , CM000668.1:g.11943872A>G GRCh37
NC_000006.10:g.12051858A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7896A>G