Canonical Allele Identifier: CA2657554339
Gene: NCAPH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50523516A>C , CM000684.2:g.50523516A>C GRCh38
NC_000022.10:g.50961945A>C , CM000684.1:g.50961945A>C GRCh37
NC_000022.9:g.49308811A>C NCBI36
NG_016235.1:g.7924T>G
NG_021419.1:g.20301A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420993.7:c.*141A>C MANE Select ENSP00000410088.2:n.*141A>C
NM_001185011.1:c.*141A>C NP_001171940.1:n.*141A>C
NM_152299.3:c.*141A>C NP_689512.2:n.*141A>C
XR_001755232.1:n.2169A>C
NM_152299.4:c.*141A>C MANE Select NP_689512.2:n.*141A>C
NM_001185011.2:c.*141A>C NP_001171940.1:n.*141A>C