Canonical Allele Identifier: CA1610684918
Gene:

Linked Data

dbSNP Id: rs1766142459

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943601A>T , CM000668.2:g.11943601A>T GRCh38
NC_000006.11:g.11943834A>T , CM000668.1:g.11943834A>T GRCh37
NC_000006.10:g.12051820A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7934A>T