Canonical Allele Identifier: CA2657554450

Gene: NCAPH2

Linked Data

• gnomAD v4: 22-50523549-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50523549G>T , CM000684.2:g.50523549G>T	GRCh38
NC_000022.10:g.50961978G>T , CM000684.1:g.50961978G>T	GRCh37
NC_000022.9:g.49308844G>T	NCBI36
NG_016235.1:g.7891C>A
NG_021419.1:g.20334G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420993.7:c.*174G>T MANE Select	ENSP00000410088.2:n.*174G>T
NM_001185011.1:c.*174G>T	NP_001171940.1:n.*174G>T
NM_152299.3:c.*174G>T	NP_689512.2:n.*174G>T
XR_001755232.1:n.2202G>T
NM_152299.4:c.*174G>T MANE Select	NP_689512.2:n.*174G>T
NM_001185011.2:c.*174G>T	NP_001171940.1:n.*174G>T