Canonical Allele Identifier: CA16385523
Gene:

Linked Data

dbSNP Id: rs2793108

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.31090176C>T , CM000672.2:g.31090176C>T GRCh38
NC_000010.10:g.31379105C>T , CM000672.1:g.31379105C>T GRCh37
NC_000010.9:g.31419111C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930796.1:n.389-15763C>T
XR_001747409.2:n.2299-15763C>T
XR_001747410.2:n.2299-15763C>T
XR_930796.2:n.878-15763C>T