Canonical Allele Identifier: CA687013257
Gene:

Linked Data

dbSNP Id: rs1460341940

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.28045324G>T , CM000674.2:g.28045324G>T GRCh38
NC_000012.11:g.28198257G>T , CM000674.1:g.28198257G>T GRCh37
NC_000012.10:g.28089524G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931460.1:n.154-6366C>A