Canonical Allele Identifier: CA731836577

Gene: MTARC2

Linked Data

• dbSNP Id: rs1466663783
• MyVariant Identifiers: chr1:g.220929257A>G (hg19) ; chr1:g.220755915A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220755915A>G , CM000663.2:g.220755915A>G	GRCh38
NC_000001.10:g.220929257A>G , CM000663.1:g.220929257A>G	GRCh37
NC_000001.9:g.218995880A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366913.8:c.446+795A>G MANE Select	ENSP00000355880.3:n.446+795A>G
ENST00000359316.6:c.446+795A>G	ENSP00000352266.2:n.446+795A>G
ENST00000366913.7:c.446+795A>G	ENSP00000355880.3:n.446+795A>G
ENST00000425560.1:c.149+795A>G	ENSP00000416442.1:n.149+795A>G
NM_017898.3:c.446+795A>G	NP_060368.2:n.446+795A>G
XM_005273168.3:c.446+795A>G	XP_005273225.1:n.446+795A>G
XM_006711407.2:c.-617A>G	XP_006711470.1:n.-617A>G
XM_011509683.1:c.-110+689A>G	XP_011507985.1:n.-110+689A>G
XM_011509684.1:c.176+795A>G	XP_011507986.1:n.176+795A>G
XR_247029.3:n.1476+795A>G
NM_001317338.1:c.446+795A>G	NP_001304267.1:n.446+795A>G
NM_001331042.1:c.446+795A>G	NP_001317971.1:n.446+795A>G
NM_017898.4:c.446+795A>G	NP_060368.2:n.446+795A>G
XR_247029.5:n.1561+795A>G
NM_017898.5:c.446+795A>G MANE Select	NP_060368.2:n.446+795A>G
NM_001317338.2:c.446+795A>G	NP_001304267.1:n.446+795A>G
NM_001331042.2:c.446+795A>G	NP_001317971.1:n.446+795A>G