Canonical Allele Identifier: CA2842489469

Gene: NCAPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50523548A>T , CM000684.2:g.50523548A>T	GRCh38
NC_000022.10:g.50961977A>T , CM000684.1:g.50961977A>T	GRCh37
NC_000022.9:g.49308843A>T	NCBI36
NG_016235.1:g.7892T>A
NG_021419.1:g.20333A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420993.7:c.*173A>T MANE Select	ENSP00000410088.2:n.*173A>T
NM_001185011.1:c.*173A>T	NP_001171940.1:n.*173A>T
NM_152299.3:c.*173A>T	NP_689512.2:n.*173A>T
XR_001755232.1:n.2201A>T
NM_152299.4:c.*173A>T MANE Select	NP_689512.2:n.*173A>T
NM_001185011.2:c.*173A>T	NP_001171940.1:n.*173A>T