Canonical Allele Identifier: CA714620951
Gene:

Linked Data

dbSNP Id: rs10519131

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61708933A>T , CM000677.2:g.61708933A>T GRCh38
NC_000015.9:g.62001132A>T , CM000677.1:g.62001132A>T GRCh37
NC_000015.8:g.59788424A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001751569.1:n.77+6182T>A