Canonical Allele Identifier: CA1610684725
Gene:

Linked Data

dbSNP Id: rs1766139539

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943360C>T , CM000668.2:g.11943360C>T GRCh38
NC_000006.11:g.11943593C>T , CM000668.1:g.11943593C>T GRCh37
NC_000006.10:g.12051579C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-8175C>T