Canonical Allele Identifier: CA284256980
Gene: MAF HGNC NCBI

Linked Data

dbSNP Id: rs1054195000
gnomAD v2: 16-79406938-C-T
gnomAD v3: 16-79373041-C-T
gnomAD v4: 16-79373041-C-T
MyVariant Identifiers: chr16:g.79406938C>T (hg19) chr16:g.79373041C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.79373041C>T , CM000678.2:g.79373041C>T GRCh38
NC_000016.9:g.79406938C>T , CM000678.1:g.79406938C>T GRCh37
NC_000016.8:g.77964439C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011523084.1:c.*29-160140G>A XP_011521386.1:n.*29-160140G>A
XM_024450279.1:c.*29-160140G>A XP_024306047.1:n.*29-160140G>A
XR_001751902.2:n.3231-160140G>A
XR_002957802.1:n.3231-160140G>A
XR_002957803.1:n.3231-160140G>A
XR_002957804.1:n.3231-160140G>A
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