Canonical Allele Identifier: CA1282864094
Gene: MARCO HGNC NCBI

Linked Data

dbSNP Id: rs1680086810
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118967961G>C , CM000664.2:g.118967961G>C GRCh38
NC_000002.11:g.119725537G>C , CM000664.1:g.119725537G>C GRCh37
NC_000002.10:g.119442007G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000327097.5:c.98-1199G>C MANE Select ENSP00000318916.4:n.98-1199G>C
ENST00000327097.4:c.98-1199G>C ENSP00000318916.4:n.98-1199G>C
ENST00000412481.1:c.-137-1199G>C ENSP00000409192.1:n.-137-1199G>C
NM_006770.3:c.98-1199G>C NP_006761.1:n.98-1199G>C
XM_011512082.1:c.98-1199G>C XP_011510384.1:n.98-1199G>C
XM_011512083.1:c.98-6372G>C XP_011510385.1:n.98-6372G>C
XM_011512082.2:c.98-1199G>C XP_011510384.1:n.98-1199G>C
XM_011512083.3:c.98-6372G>C XP_011510385.1:n.98-6372G>C
XM_017005171.2:c.98-1199G>C XP_016860660.1:n.98-1199G>C
NM_006770.4:c.98-1199G>C MANE Select NP_006761.1:n.98-1199G>C
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