Canonical Allele Identifier: CA2624417406

Gene: GZMB

Linked Data

• gnomAD v4: 14-24632760-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632764del , CM000676.2:g.24632764del	GRCh38
NC_000014.8:g.25101970del , CM000676.1:g.25101970del	GRCh37
NC_000014.7:g.24171810del	NCBI36
NG_028340.1:g.6466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216341.9:c.203+154del MANE Select	ENSP00000216341.4:n.203+154del
ENST00000216341.8:c.203+154del	ENSP00000216341.4:n.203+154del
ENST00000382540.5:c.204-42del	ENSP00000371980.1:n.204-42del
ENST00000382542.5:c.203+154del	ENSP00000371982.2:n.203+154del
ENST00000415355.7:c.167+154del	ENSP00000387385.3:n.167+154del
ENST00000526004.1:c.203+154del	ENSP00000434213.1:n.203+154del
ENST00000530830.1:c.*126+154del	ENSP00000435084.1:n.*126+154del
ENST00000532263.5:c.56-643del	ENSP00000432074.1:n.56-643del
ENST00000554242.5:c.203+154del	ENSP00000450535.1:n.203+154del
ENST00000616551.1:c.52-640del	ENSP00000479643.1:n.52-640del
NM_004131.4:c.203+154del	NP_004122.2:n.203+154del
XM_011536685.1:c.167+154del	XP_011534987.1:n.167+154del
NM_001346011.1:c.167+154del	NP_001332940.1:n.167+154del
NM_004131.5:c.203+154del	NP_004122.2:n.203+154del
NR_144343.1:n.312+154del
NM_004131.6:c.203+154del MANE Select	NP_004122.2:n.203+154del
NM_001346011.2:c.167+154del	NP_001332940.1:n.167+154del
NR_144343.2:n.233+154del