Canonical Allele Identifier: CA1250829427
Gene:

Linked Data

dbSNP Id: rs1668662673

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722498C>G , CM000664.2:g.52722498C>G GRCh38
NC_000002.11:g.52949636C>G , CM000664.1:g.52949636C>G GRCh37
NC_000002.10:g.52803140C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.759G>C