Canonical Allele Identifier: CA1035566701
Gene: MARCO HGNC NCBI

Linked Data

dbSNP Id: rs1680080833
gnomAD v3: 2-118967797-T-C
gnomAD v4: 2-118967797-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118967797T>C , CM000664.2:g.118967797T>C GRCh38
NC_000002.11:g.119725373T>C , CM000664.1:g.119725373T>C GRCh37
NC_000002.10:g.119441843T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000327097.5:c.98-1363T>C MANE Select ENSP00000318916.4:n.98-1363T>C
ENST00000327097.4:c.98-1363T>C ENSP00000318916.4:n.98-1363T>C
ENST00000412481.1:c.-137-1363T>C ENSP00000409192.1:n.-137-1363T>C
NM_006770.3:c.98-1363T>C NP_006761.1:n.98-1363T>C
XM_011512082.1:c.98-1363T>C XP_011510384.1:n.98-1363T>C
XM_011512083.1:c.98-6536T>C XP_011510385.1:n.98-6536T>C
XM_011512082.2:c.98-1363T>C XP_011510384.1:n.98-1363T>C
XM_011512083.3:c.98-6536T>C XP_011510385.1:n.98-6536T>C
XM_017005171.2:c.98-1363T>C XP_016860660.1:n.98-1363T>C
NM_006770.4:c.98-1363T>C MANE Select NP_006761.1:n.98-1363T>C
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