Canonical Allele Identifier: CA54572382

Gene: MARCO

Linked Data

• dbSNP Id: rs956428159
• gnomAD v3: 2-118967960-A-G
• gnomAD v4: 2-118967960-A-G
• MyVariant Identifiers: chr2:g.119725536A>G (hg19) ; chr2:g.118967960A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118967960A>G , CM000664.2:g.118967960A>G	GRCh38
NC_000002.11:g.119725536A>G , CM000664.1:g.119725536A>G	GRCh37
NC_000002.10:g.119442006A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000327097.5:c.98-1200A>G MANE Select	ENSP00000318916.4:n.98-1200A>G
ENST00000327097.4:c.98-1200A>G	ENSP00000318916.4:n.98-1200A>G
ENST00000412481.1:c.-137-1200A>G	ENSP00000409192.1:n.-137-1200A>G
NM_006770.3:c.98-1200A>G	NP_006761.1:n.98-1200A>G
XM_011512082.1:c.98-1200A>G	XP_011510384.1:n.98-1200A>G
XM_011512083.1:c.98-6373A>G	XP_011510385.1:n.98-6373A>G
XM_011512082.2:c.98-1200A>G	XP_011510384.1:n.98-1200A>G
XM_011512083.3:c.98-6373A>G	XP_011510385.1:n.98-6373A>G
XM_017005171.2:c.98-1200A>G	XP_016860660.1:n.98-1200A>G
NM_006770.4:c.98-1200A>G MANE Select	NP_006761.1:n.98-1200A>G