Canonical Allele Identifier: CA54572231
Gene: MARCO HGNC NCBI

Linked Data

dbSNP Id: rs566151077
gnomAD v2: 2-119725379-C-A
gnomAD v3: 2-118967803-C-A
gnomAD v4: 2-118967803-C-A
MyVariant Identifiers: chr2:g.119725379C>A (hg19) chr2:g.118967803C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118967803C>A , CM000664.2:g.118967803C>A GRCh38
NC_000002.11:g.119725379C>A , CM000664.1:g.119725379C>A GRCh37
NC_000002.10:g.119441849C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000327097.5:c.98-1357C>A MANE Select ENSP00000318916.4:n.98-1357C>A
ENST00000327097.4:c.98-1357C>A ENSP00000318916.4:n.98-1357C>A
ENST00000412481.1:c.-137-1357C>A ENSP00000409192.1:n.-137-1357C>A
NM_006770.3:c.98-1357C>A NP_006761.1:n.98-1357C>A
XM_011512082.1:c.98-1357C>A XP_011510384.1:n.98-1357C>A
XM_011512083.1:c.98-6530C>A XP_011510385.1:n.98-6530C>A
XM_011512082.2:c.98-1357C>A XP_011510384.1:n.98-1357C>A
XM_011512083.3:c.98-6530C>A XP_011510385.1:n.98-6530C>A
XM_017005171.2:c.98-1357C>A XP_016860660.1:n.98-1357C>A
NM_006770.4:c.98-1357C>A MANE Select NP_006761.1:n.98-1357C>A
Search 100 bp 5'
Search 100 bp 3'