Canonical Allele Identifier: CA2657554319
Gene: NCAPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50523508C>T , CM000684.2:g.50523508C>T GRCh38
NC_000022.10:g.50961937C>T , CM000684.1:g.50961937C>T GRCh37
NC_000022.9:g.49308803C>T NCBI36
NG_016235.1:g.7932G>A
NG_021419.1:g.20293C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000420993.7:c.*133C>T MANE Select ENSP00000410088.2:n.*133C>T
NM_001185011.1:c.*133C>T NP_001171940.1:n.*133C>T
NM_152299.3:c.*133C>T NP_689512.2:n.*133C>T
XR_001755232.1:n.2161C>T
NM_152299.4:c.*133C>T MANE Select NP_689512.2:n.*133C>T
NM_001185011.2:c.*133C>T NP_001171940.1:n.*133C>T