Canonical Allele Identifier: CA1250829402
Gene:

Linked Data

dbSNP Id: rs1668657638

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722450G>C , CM000664.2:g.52722450G>C GRCh38
NC_000002.11:g.52949588G>C , CM000664.1:g.52949588G>C GRCh37
NC_000002.10:g.52803092G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.807C>G