Canonical Allele Identifier: CA325554928

Gene: SCO2 NCAPH2

Linked Data

• dbSNP Id: rs1011393334
• gnomAD v3: 22-50523573-C-T
• gnomAD v4: 22-50523573-C-T
• MyVariant Identifiers: chr22:g.50962002C>T (hg19) ; chr22:g.50523573C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50523573C>T , CM000684.2:g.50523573C>T	GRCh38
NC_000022.10:g.50962002C>T , CM000684.1:g.50962002C>T	GRCh37
NC_000022.9:g.49308868C>T	NCBI36
NG_016235.1:g.7867G>A
NG_021419.1:g.20358C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395693.8:c.*38G>A (SCO2) MANE Select	ENSP00000379046.4:n.*38G>A
ENST00000420993.7:c.*198C>T (NCAPH2) MANE Select	ENSP00000410088.2:n.*198C>T
ENST00000543927.6:c.*38G>A (SCO2)	ENSP00000444433.1:n.*38G>A
ENST00000395693.7:c.*38G>A	ENSP00000379046.3:n.*38G>A
ENST00000535425.5:c.*38G>A	ENSP00000444242.1:n.*38G>A
ENST00000543927.5:c.*38G>A	ENSP00000444433.1:n.*38G>A
NM_001169109.1:c.*38G>A (SCO2)	NP_001162580.1:n.*38G>A
NM_001169110.1:c.*38G>A (SCO2)	NP_001162581.1:n.*38G>A
NM_001169111.1:c.*38G>A (SCO2)	NP_001162582.1:n.*38G>A
NM_001185011.1:c.*198C>T (NCAPH2)	NP_001171940.1:n.*198C>T
NM_005138.2:c.*38G>A (SCO2)	NP_005129.2:n.*38G>A
NM_152299.3:c.*198C>T (NCAPH2)	NP_689512.2:n.*198C>T
XR_001755232.1:n.2226C>T (NCAPH2)
NM_152299.4:c.*198C>T (NCAPH2) MANE Select	NP_689512.2:n.*198C>T
NM_001185011.2:c.*198C>T (NCAPH2)	NP_001171940.1:n.*198C>T
NM_005138.3:c.*38G>A (SCO2) MANE Select	NP_005129.2:n.*38G>A
NM_001169109.2:c.*38G>A (SCO2)	NP_001162580.1:n.*38G>A
NM_001169111.2:c.*38G>A (SCO2)	NP_001162582.1:n.*38G>A