Canonical Allele Identifier: CA10321303

Gene: SCO2 NCAPH2

Linked Data

• ClinVar Variation Id: 3007126
• ClinVar RCV Id: RCV003868765
• dbSNP Id: rs768107740
• ExAC: 22:50962775 G / A
• gnomAD v2: 22-50962775-G-A
• gnomAD v3: 22-50524346-G-A
• gnomAD v4: 22-50524346-G-A
• MyVariant Identifiers: chr22:g.50962775G>A (hg19) ; chr22:g.50524346G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50524346G>A , CM000684.2:g.50524346G>A	GRCh38
NC_000022.10:g.50962775G>A , CM000684.1:g.50962775G>A	GRCh37
NC_000022.9:g.49309641G>A	NCBI36
NG_011860.1:g.10740C>T , LRG_727:g.10740C>T
NG_016235.1:g.7094C>T
NG_021419.1:g.21131G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395693.8:c.66C>T (SCO2) MANE Select	ENSP00000379046.4:p.Leu22=
ENST00000420993.7:c.*971G>A (NCAPH2) MANE Select	ENSP00000410088.2:n.*971G>A
ENST00000543927.6:c.66C>T (SCO2)	ENSP00000444433.1:p.Leu22=
ENST00000638598.2:c.66C>T (SCO2)	ENSP00000491753.2:p.Leu22=
ENST00000252785.3:c.66C>T	ENSP00000252785.3:p.Leu22=
ENST00000395693.7:c.66C>T	ENSP00000379046.3:p.Leu22=
ENST00000423348.1:c.66C>T	ENSP00000403570.1:p.Leu22=
ENST00000439934.5:c.66C>T	ENSP00000415642.1:p.Leu22=
ENST00000535425.5:c.66C>T	ENSP00000444242.1:p.Leu22=
ENST00000543927.5:c.66C>T	ENSP00000444433.1:p.Leu22=
NM_001169109.1:c.66C>T (SCO2)	NP_001162580.1:p.Leu22=
NM_001169110.1:c.66C>T (SCO2)	NP_001162581.1:p.Leu22=
NM_001169111.1:c.66C>T (SCO2)	NP_001162582.1:p.Leu22=
NM_001185011.1:c.*971G>A (NCAPH2)	NP_001171940.1:n.*971G>A
NM_005138.2:c.66C>T (SCO2)	NP_005129.2:p.Leu22=
NM_152299.3:c.*971G>A (NCAPH2)	NP_689512.2:n.*971G>A
XR_001755232.1:n.2999G>A (NCAPH2)
NM_152299.4:c.*971G>A (NCAPH2) MANE Select	NP_689512.2:n.*971G>A
NM_001185011.2:c.*971G>A (NCAPH2)	NP_001171940.1:n.*971G>A
NM_005138.3:c.66C>T (SCO2) MANE Select	NP_005129.2:p.Leu22=
NM_001169109.2:c.66C>T (SCO2)	NP_001162580.1:p.Leu22=
NM_001169111.2:c.66C>T (SCO2)	NP_001162582.1:p.Leu22=