Canonical Allele Identifier: CA1610684710
Gene:

Linked Data

dbSNP Id: rs368931217

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943348A>C , CM000668.2:g.11943348A>C GRCh38
NC_000006.11:g.11943581A>C , CM000668.1:g.11943581A>C GRCh37
NC_000006.10:g.12051567A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-8187A>C