Canonical Allele Identifier: CA11026707

Gene: MARCO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118985008C>T , CM000664.2:g.118985008C>T	GRCh38
NC_000002.11:g.119742584C>T , CM000664.1:g.119742584C>T	GRCh37
NC_000002.10:g.119459054C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327097.5:c.1063+2598C>T MANE Select	ENSP00000318916.4:n.1063+2598C>T
ENST00000327097.4:c.1063+2598C>T	ENSP00000318916.4:n.1063+2598C>T
NM_006770.3:c.1063+2598C>T	NP_006761.1:n.1063+2598C>T
XM_011512082.1:c.1063+2598C>T	XP_011510384.1:n.1063+2598C>T
XM_011512083.1:c.700+2598C>T	XP_011510385.1:n.700+2598C>T
XM_011512082.2:c.1063+2598C>T	XP_011510384.1:n.1063+2598C>T
XM_011512083.3:c.700+2598C>T	XP_011510385.1:n.700+2598C>T
NM_006770.4:c.1063+2598C>T MANE Select	NP_006761.1:n.1063+2598C>T