Canonical Allele Identifier: CA2657554333
Gene: NCAPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50523513A>G , CM000684.2:g.50523513A>G GRCh38
NC_000022.10:g.50961942A>G , CM000684.1:g.50961942A>G GRCh37
NC_000022.9:g.49308808A>G NCBI36
NG_016235.1:g.7927T>C
NG_021419.1:g.20298A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000420993.7:c.*138A>G MANE Select ENSP00000410088.2:n.*138A>G
NM_001185011.1:c.*138A>G NP_001171940.1:n.*138A>G
NM_152299.3:c.*138A>G NP_689512.2:n.*138A>G
XR_001755232.1:n.2166A>G
NM_152299.4:c.*138A>G MANE Select NP_689512.2:n.*138A>G
NM_001185011.2:c.*138A>G NP_001171940.1:n.*138A>G