Canonical Allele Identifier: CA2235789664
Gene: MAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.79373086A= , CM000678.2:g.79373086A= GRCh38
NC_000016.9:g.79406983A= , CM000678.1:g.79406983A= GRCh37
NC_000016.8:g.77964484A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011523084.1:c.*29-160185T= XP_011521386.1:n.*29-160185T=
XM_024450279.1:c.*29-160185T= XP_024306047.1:n.*29-160185T=
XR_001751902.2:n.3231-160185T=
XR_002957802.1:n.3231-160185T=
XR_002957803.1:n.3231-160185T=
XR_002957804.1:n.3231-160185T=