Canonical Allele Identifier: CA2699235114
Gene:

Linked Data

dbSNP Id: rs2103801369

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722382C>G , CM000664.2:g.52722382C>G GRCh38
NC_000002.11:g.52949520C>G , CM000664.1:g.52949520C>G GRCh37
NC_000002.10:g.52803024C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.875G>C