Canonical Allele Identifier: CA11026705
Gene: MARCO HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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