Canonical Allele Identifier: CA2410905762
Gene: NCAPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50523560C= , CM000684.2:g.50523560C= GRCh38
NC_000022.10:g.50961989C= , CM000684.1:g.50961989C= GRCh37
NC_000022.9:g.49308855C= NCBI36
NG_016235.1:g.7880G=
NG_021419.1:g.20345C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420993.7:c.*185C= MANE Select ENSP00000410088.2:n.*185C=
NM_001185011.1:c.*185C= NP_001171940.1:n.*185C=
NM_152299.3:c.*185C= NP_689512.2:n.*185C=
XR_001755232.1:n.2213C=
NM_152299.4:c.*185C= MANE Select NP_689512.2:n.*185C=
NM_001185011.2:c.*185C= NP_001171940.1:n.*185C=
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