Canonical Allele Identifier: CA1948159631
Gene:

Linked Data

dbSNP Id: rs1353000574

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444555C>G , CM000673.2:g.2444555C>G GRCh38
NC_000011.9:g.2465785C>G , CM000673.1:g.2465785C>G GRCh37
NC_000011.8:g.2422361C>G NCBI36
NG_008935.1:g.4565C>G , LRG_287:g.4565C>G

Transcript Alleles

HGVS Amino-acid Change
XR_930984.1:n.16G>C