Canonical Allele Identifier: CA2657554367
Gene: NCAPH2 HGNC NCBI

Linked Data

gnomAD v4: 22-50523525-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50523525T>G , CM000684.2:g.50523525T>G GRCh38
NC_000022.10:g.50961954T>G , CM000684.1:g.50961954T>G GRCh37
NC_000022.9:g.49308820T>G NCBI36
NG_016235.1:g.7915A>C
NG_021419.1:g.20310T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000420993.7:c.*150T>G MANE Select ENSP00000410088.2:n.*150T>G
NM_001185011.1:c.*150T>G NP_001171940.1:n.*150T>G
NM_152299.3:c.*150T>G NP_689512.2:n.*150T>G
XR_001755232.1:n.2178T>G
NM_152299.4:c.*150T>G MANE Select NP_689512.2:n.*150T>G
NM_001185011.2:c.*150T>G NP_001171940.1:n.*150T>G
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