Canonical Allele Identifier: CA1035566743
Gene: MARCO HGNC NCBI

Linked Data

dbSNP Id: rs1680088445
gnomAD v3: 2-118968000-G-A
gnomAD v4: 2-118968000-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118968000G>A , CM000664.2:g.118968000G>A GRCh38
NC_000002.11:g.119725576G>A , CM000664.1:g.119725576G>A GRCh37
NC_000002.10:g.119442046G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000327097.5:c.98-1160G>A MANE Select ENSP00000318916.4:n.98-1160G>A
ENST00000327097.4:c.98-1160G>A ENSP00000318916.4:n.98-1160G>A
ENST00000412481.1:c.-137-1160G>A ENSP00000409192.1:n.-137-1160G>A
NM_006770.3:c.98-1160G>A NP_006761.1:n.98-1160G>A
XM_011512082.1:c.98-1160G>A XP_011510384.1:n.98-1160G>A
XM_011512083.1:c.98-6333G>A XP_011510385.1:n.98-6333G>A
XM_011512082.2:c.98-1160G>A XP_011510384.1:n.98-1160G>A
XM_011512083.3:c.98-6333G>A XP_011510385.1:n.98-6333G>A
XM_017005171.2:c.98-1160G>A XP_016860660.1:n.98-1160G>A
NM_006770.4:c.98-1160G>A MANE Select NP_006761.1:n.98-1160G>A
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