Canonical Allele Identifier: CA16109698

Gene: MARCO

Linked Data

• dbSNP Id: rs12998782
• gnomAD v2: 2-119725380-C-T
• gnomAD v3: 2-118967804-C-T
• gnomAD v4: 2-118967804-C-T
• MyVariant Identifiers: chr2:g.119725380C>T (hg19) ; chr2:g.118967804C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118967804C>T , CM000664.2:g.118967804C>T	GRCh38
NC_000002.11:g.119725380C>T , CM000664.1:g.119725380C>T	GRCh37
NC_000002.10:g.119441850C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000327097.5:c.98-1356C>T MANE Select	ENSP00000318916.4:n.98-1356C>T
ENST00000327097.4:c.98-1356C>T	ENSP00000318916.4:n.98-1356C>T
ENST00000412481.1:c.-137-1356C>T	ENSP00000409192.1:n.-137-1356C>T
NM_006770.3:c.98-1356C>T	NP_006761.1:n.98-1356C>T
XM_011512082.1:c.98-1356C>T	XP_011510384.1:n.98-1356C>T
XM_011512083.1:c.98-6529C>T	XP_011510385.1:n.98-6529C>T
XM_011512082.2:c.98-1356C>T	XP_011510384.1:n.98-1356C>T
XM_011512083.3:c.98-6529C>T	XP_011510385.1:n.98-6529C>T
XM_017005171.2:c.98-1356C>T	XP_016860660.1:n.98-1356C>T
NM_006770.4:c.98-1356C>T MANE Select	NP_006761.1:n.98-1356C>T