Canonical Allele Identifier: CA2235789599
Gene: MAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.79373024G= , CM000678.2:g.79373024G= GRCh38
NC_000016.9:g.79406921G= , CM000678.1:g.79406921G= GRCh37
NC_000016.8:g.77964422G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011523084.1:c.*29-160123C= XP_011521386.1:n.*29-160123C=
XM_024450279.1:c.*29-160123C= XP_024306047.1:n.*29-160123C=
XR_001751902.2:n.3231-160123C=
XR_002957802.1:n.3231-160123C=
XR_002957803.1:n.3231-160123C=
XR_002957804.1:n.3231-160123C=