Canonical Allele Identifier: CA1035566778
Gene: MARCO HGNC NCBI

Linked Data

dbSNP Id: rs1573389395

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118968167G>T , CM000664.2:g.118968167G>T GRCh38
NC_000002.11:g.119725743G>T , CM000664.1:g.119725743G>T GRCh37
NC_000002.10:g.119442213G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000327097.5:c.98-993G>T MANE Select ENSP00000318916.4:n.98-993G>T
ENST00000327097.4:c.98-993G>T ENSP00000318916.4:n.98-993G>T
ENST00000412481.1:c.-137-993G>T ENSP00000409192.1:n.-137-993G>T
NM_006770.3:c.98-993G>T NP_006761.1:n.98-993G>T
XM_011512082.1:c.98-993G>T XP_011510384.1:n.98-993G>T
XM_011512083.1:c.98-6166G>T XP_011510385.1:n.98-6166G>T
XM_011512082.2:c.98-993G>T XP_011510384.1:n.98-993G>T
XM_011512083.3:c.98-6166G>T XP_011510385.1:n.98-6166G>T
XM_017005171.2:c.98-993G>T XP_016860660.1:n.98-993G>T
NM_006770.4:c.98-993G>T MANE Select NP_006761.1:n.98-993G>T