Canonical Allele Identifier: CA1282867737
Gene: MARCO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118975372G= , CM000664.2:g.118975372G= GRCh38
NC_000002.11:g.119732948G= , CM000664.1:g.119732948G= GRCh37
NC_000002.10:g.119449418G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000327097.5:c.613+807G= MANE Select ENSP00000318916.4:n.613+807G=
ENST00000327097.4:c.613+807G= ENSP00000318916.4:n.613+807G=
NM_006770.3:c.613+807G= NP_006761.1:n.613+807G=
XM_011512082.1:c.613+807G= XP_011510384.1:n.613+807G=
XM_011512083.1:c.250+807G= XP_011510385.1:n.250+807G=
XM_011512082.2:c.613+807G= XP_011510384.1:n.613+807G=
XM_011512083.3:c.250+807G= XP_011510385.1:n.250+807G=
XM_017005171.2:c.613+807G= XP_016860660.1:n.613+807G=
NM_006770.4:c.613+807G= MANE Select NP_006761.1:n.613+807G=