Canonical Allele Identifier: CA37598954

Gene: MTARC2

Linked Data

• dbSNP Id: rs896076026
• gnomAD v3: 1-220755969-G-A
• gnomAD v4: 1-220755969-G-A
• MyVariant Identifiers: chr1:g.220929311G>A (hg19) ; chr1:g.220755969G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220755969G>A , CM000663.2:g.220755969G>A	GRCh38
NC_000001.10:g.220929311G>A , CM000663.1:g.220929311G>A	GRCh37
NC_000001.9:g.218995934G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366913.8:c.446+849G>A MANE Select	ENSP00000355880.3:n.446+849G>A
ENST00000359316.6:c.446+849G>A	ENSP00000352266.2:n.446+849G>A
ENST00000366913.7:c.446+849G>A	ENSP00000355880.3:n.446+849G>A
ENST00000425560.1:c.149+849G>A	ENSP00000416442.1:n.149+849G>A
NM_017898.3:c.446+849G>A	NP_060368.2:n.446+849G>A
XM_005273168.3:c.446+849G>A	XP_005273225.1:n.446+849G>A
XM_006711407.2:c.-563G>A	XP_006711470.1:n.-563G>A
XM_011509683.1:c.-110+743G>A	XP_011507985.1:n.-110+743G>A
XM_011509684.1:c.176+849G>A	XP_011507986.1:n.176+849G>A
XR_247029.3:n.1476+849G>A
NM_001317338.1:c.446+849G>A	NP_001304267.1:n.446+849G>A
NM_001331042.1:c.446+849G>A	NP_001317971.1:n.446+849G>A
NM_017898.4:c.446+849G>A	NP_060368.2:n.446+849G>A
XR_247029.5:n.1561+849G>A
NM_017898.5:c.446+849G>A MANE Select	NP_060368.2:n.446+849G>A
NM_001317338.2:c.446+849G>A	NP_001304267.1:n.446+849G>A
NM_001331042.2:c.446+849G>A	NP_001317971.1:n.446+849G>A