Canonical Allele Identifier: CA1833676231
Gene:

Linked Data

dbSNP Id: rs1824907489

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12108838A>T , CM000671.2:g.12108838A>T GRCh38
NC_000009.11:g.12108838A>T , CM000671.1:g.12108838A>T GRCh37
NC_000009.10:g.12098838A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929481.1:n.166+7983T>A
XR_929482.1:n.260+7983T>A
XR_929481.2:n.166+7983T>A
XR_929482.2:n.260+7983T>A