Canonical Allele Identifier: CA2235910980
Gene: MAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.79551124C>G , CM000678.2:g.79551124C>G GRCh38
NC_000016.9:g.79585021C>G , CM000678.1:g.79585021C>G GRCh37
NC_000016.8:g.78142522C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011523084.1:c.*28+34756G>C XP_011521386.1:n.*28+34756G>C
XM_024450279.1:c.*28+34756G>C XP_024306047.1:n.*28+34756G>C
XR_001751902.2:n.3230+34756G>C
XR_002957802.1:n.3230+34756G>C
XR_002957803.1:n.3230+34756G>C
XR_002957804.1:n.3230+34756G>C