Canonical Allele Identifier: CA862161280
Gene:

Linked Data

dbSNP Id: rs1246975002

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21755965C>T , CM000671.2:g.21755965C>T GRCh38
NC_000009.11:g.21755964C>T , CM000671.1:g.21755964C>T GRCh37
NC_000009.10:g.21745964C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11860G>A