Canonical Allele Identifier: CA778454177
Gene:

Linked Data

dbSNP Id: rs114528045

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756534G>T , CM000680.2:g.31756534G>T GRCh38
NC_000018.9:g.29336497G>T , CM000680.1:g.29336497G>T GRCh37
NC_000018.8:g.27590495G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5605G>T