Canonical Allele Identifier: CA1282864119
Gene: MARCO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118968001T= , CM000664.2:g.118968001T= GRCh38
NC_000002.11:g.119725577T= , CM000664.1:g.119725577T= GRCh37
NC_000002.10:g.119442047T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000327097.5:c.98-1159T= MANE Select ENSP00000318916.4:n.98-1159T=
ENST00000327097.4:c.98-1159T= ENSP00000318916.4:n.98-1159T=
ENST00000412481.1:c.-137-1159T= ENSP00000409192.1:n.-137-1159T=
NM_006770.3:c.98-1159T= NP_006761.1:n.98-1159T=
XM_011512082.1:c.98-1159T= XP_011510384.1:n.98-1159T=
XM_011512083.1:c.98-6332T= XP_011510385.1:n.98-6332T=
XM_011512082.2:c.98-1159T= XP_011510384.1:n.98-1159T=
XM_011512083.3:c.98-6332T= XP_011510385.1:n.98-6332T=
XM_017005171.2:c.98-1159T= XP_016860660.1:n.98-1159T=
NM_006770.4:c.98-1159T= MANE Select NP_006761.1:n.98-1159T=