Canonical Allele Identifier: CA15886042
Gene: MAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.79405477A>G , CM000678.2:g.79405477A>G GRCh38
NC_000016.9:g.79439374A>G , CM000678.1:g.79439374A>G GRCh37
NC_000016.8:g.77996875A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011523084.1:c.*28+180403T>C XP_011521386.1:n.*28+180403T>C
XM_024450279.1:c.*28+180403T>C XP_024306047.1:n.*28+180403T>C
XR_001751902.2:n.3230+180403T>C
XR_002957802.1:n.3230+180403T>C
XR_002957803.1:n.3230+180403T>C
XR_002957804.1:n.3230+180403T>C