Canonical Allele Identifier: CA284256968

Gene: MAF

Linked Data

• dbSNP Id: rs17797882
• gnomAD v2: 16-79406918-C-T
• gnomAD v3: 16-79373021-C-T
• gnomAD v4: 16-79373021-C-T
• MyVariant Identifiers: chr16:g.79406918C>T (hg19) ; chr16:g.79373021C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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