Canonical Allele Identifier: CA693572551
Gene:

Linked Data

dbSNP Id: rs1462560193

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293206T>C , CM000674.2:g.93293206T>C GRCh38
NC_000012.11:g.93686982T>C , CM000674.1:g.93686982T>C GRCh37
NC_000012.10:g.92211113T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34821A>G