Canonical Allele Identifier: CA755826865

Gene: MARCO

Linked Data

• dbSNP Id: rs1251528737
• gnomAD v3: 2-118967886-A-G
• gnomAD v4: 2-118967886-A-G
• MyVariant Identifiers: chr2:g.119725462A>G (hg19) ; chr2:g.118967886A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118967886A>G , CM000664.2:g.118967886A>G	GRCh38
NC_000002.11:g.119725462A>G , CM000664.1:g.119725462A>G	GRCh37
NC_000002.10:g.119441932A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000327097.5:c.98-1274A>G MANE Select	ENSP00000318916.4:n.98-1274A>G
ENST00000327097.4:c.98-1274A>G	ENSP00000318916.4:n.98-1274A>G
ENST00000412481.1:c.-137-1274A>G	ENSP00000409192.1:n.-137-1274A>G
NM_006770.3:c.98-1274A>G	NP_006761.1:n.98-1274A>G
XM_011512082.1:c.98-1274A>G	XP_011510384.1:n.98-1274A>G
XM_011512083.1:c.98-6447A>G	XP_011510385.1:n.98-6447A>G
XM_011512082.2:c.98-1274A>G	XP_011510384.1:n.98-1274A>G
XM_011512083.3:c.98-6447A>G	XP_011510385.1:n.98-6447A>G
XM_017005171.2:c.98-1274A>G	XP_016860660.1:n.98-1274A>G
NM_006770.4:c.98-1274A>G MANE Select	NP_006761.1:n.98-1274A>G