Canonical Allele Identifier: CA241972488
Gene:

Linked Data

dbSNP Id: rs979645210

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293124T>C , CM000674.2:g.93293124T>C GRCh38
NC_000012.11:g.93686900T>C , CM000674.1:g.93686900T>C GRCh37
NC_000012.10:g.92211031T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34903A>G