Canonical Allele Identifier: CA724410806
Gene: MAF HGNC NCBI

Linked Data

dbSNP Id: rs17797882

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.79373021C>G , CM000678.2:g.79373021C>G GRCh38
NC_000016.9:g.79406918C>G , CM000678.1:g.79406918C>G GRCh37
NC_000016.8:g.77964419C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011523084.1:c.*29-160120G>C XP_011521386.1:n.*29-160120G>C
XM_024450279.1:c.*29-160120G>C XP_024306047.1:n.*29-160120G>C
XR_001751902.2:n.3231-160120G>C
XR_002957802.1:n.3231-160120G>C
XR_002957803.1:n.3231-160120G>C
XR_002957804.1:n.3231-160120G>C