Canonical Allele Identifier: CA2790193546
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444536A>C , CM000673.2:g.2444536A>C GRCh38
NC_000011.9:g.2465766A>C , CM000673.1:g.2465766A>C GRCh37
NC_000011.8:g.2422342A>C NCBI36
NG_008935.1:g.4546A>C , LRG_287:g.4546A>C

Transcript Alleles

HGVS Amino-acid Change
XR_930984.1:n.35T>G