Canonical Allele Identifier: CA1563552190
Gene:

Linked Data

dbSNP Id: rs1346680373

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222997A>T , CM000667.2:g.92222997A>T GRCh38
NC_000005.9:g.91518814A>T , CM000667.1:g.91518814A>T GRCh37
NC_000005.8:g.91554570A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18313A>T