Canonical Allele Identifier: CA2657554380
Gene: NCAPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50523529C>A , CM000684.2:g.50523529C>A GRCh38
NC_000022.10:g.50961958C>A , CM000684.1:g.50961958C>A GRCh37
NC_000022.9:g.49308824C>A NCBI36
NG_016235.1:g.7911G>T
NG_021419.1:g.20314C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420993.7:c.*154C>A MANE Select ENSP00000410088.2:n.*154C>A
NM_001185011.1:c.*154C>A NP_001171940.1:n.*154C>A
NM_152299.3:c.*154C>A NP_689512.2:n.*154C>A
XR_001755232.1:n.2182C>A
NM_152299.4:c.*154C>A MANE Select NP_689512.2:n.*154C>A
NM_001185011.2:c.*154C>A NP_001171940.1:n.*154C>A