Canonical Allele Identifier: CA847118732
Gene:

Linked Data

dbSNP Id: rs1198177036

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127012506A>T , CM000670.2:g.127012506A>T GRCh38
NC_000008.10:g.128024751A>T , CM000670.1:g.128024751A>T GRCh37
NC_000008.9:g.128093933A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1364+5888A>T