Canonical Allele Identifier: CA54572664

Gene: MARCO

Linked Data

• dbSNP Id: rs1024324347
• gnomAD v2: 2-119725796-C-T
• gnomAD v3: 2-118968220-C-T
• gnomAD v4: 2-118968220-C-T
• COSMIC: COSN22064963
• MyVariant Identifiers: chr2:g.119725796C>T (hg19) ; chr2:g.118968220C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118968220C>T , CM000664.2:g.118968220C>T	GRCh38
NC_000002.11:g.119725796C>T , CM000664.1:g.119725796C>T	GRCh37
NC_000002.10:g.119442266C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327097.5:c.98-940C>T MANE Select	ENSP00000318916.4:n.98-940C>T
ENST00000327097.4:c.98-940C>T	ENSP00000318916.4:n.98-940C>T
ENST00000412481.1:c.-137-940C>T	ENSP00000409192.1:n.-137-940C>T
NM_006770.3:c.98-940C>T	NP_006761.1:n.98-940C>T
XM_011512082.1:c.98-940C>T	XP_011510384.1:n.98-940C>T
XM_011512083.1:c.98-6113C>T	XP_011510385.1:n.98-6113C>T
XM_011512082.2:c.98-940C>T	XP_011510384.1:n.98-940C>T
XM_011512083.3:c.98-6113C>T	XP_011510385.1:n.98-6113C>T
XM_017005171.2:c.98-940C>T	XP_016860660.1:n.98-940C>T
NM_006770.4:c.98-940C>T MANE Select	NP_006761.1:n.98-940C>T