Canonical Allele Identifier: CA2410905753
Gene: NCAPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50523540G= , CM000684.2:g.50523540G= GRCh38
NC_000022.10:g.50961969G= , CM000684.1:g.50961969G= GRCh37
NC_000022.9:g.49308835G= NCBI36
NG_016235.1:g.7900C=
NG_021419.1:g.20325G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420993.7:c.*165G= MANE Select ENSP00000410088.2:n.*165G=
NM_001185011.1:c.*165G= NP_001171940.1:n.*165G=
NM_152299.3:c.*165G= NP_689512.2:n.*165G=
XR_001755232.1:n.2193G=
NM_152299.4:c.*165G= MANE Select NP_689512.2:n.*165G=
NM_001185011.2:c.*165G= NP_001171940.1:n.*165G=