Canonical Allele Identifier: CA2624417509

Gene: GZMB

Linked Data

• gnomAD v4: 14-24632893-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632893T>C , CM000676.2:g.24632893T>C	GRCh38
NC_000014.8:g.25102099T>C , CM000676.1:g.25102099T>C	GRCh37
NC_000014.7:g.24171939T>C	NCBI36
NG_028340.1:g.6334A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216341.9:c.203+22A>G MANE Select	ENSP00000216341.4:n.203+22A>G
ENST00000216341.8:c.203+22A>G	ENSP00000216341.4:n.203+22A>G
ENST00000382540.5:c.203+22A>G	ENSP00000371980.1:n.203+22A>G
ENST00000382542.5:c.203+22A>G	ENSP00000371982.2:n.203+22A>G
ENST00000415355.7:c.167+22A>G	ENSP00000387385.3:n.167+22A>G
ENST00000526004.1:c.203+22A>G	ENSP00000434213.1:n.203+22A>G
ENST00000530830.1:c.*126+22A>G	ENSP00000435084.1:n.*126+22A>G
ENST00000532263.5:c.56-775A>G	ENSP00000432074.1:n.56-775A>G
ENST00000554242.5:c.203+22A>G	ENSP00000450535.1:n.203+22A>G
ENST00000616551.1:c.52-772A>G	ENSP00000479643.1:n.52-772A>G
NM_004131.4:c.203+22A>G	NP_004122.2:n.203+22A>G
XM_011536685.1:c.167+22A>G	XP_011534987.1:n.167+22A>G
NM_001346011.1:c.167+22A>G	NP_001332940.1:n.167+22A>G
NM_004131.5:c.203+22A>G	NP_004122.2:n.203+22A>G
NR_144343.1:n.312+22A>G
NM_004131.6:c.203+22A>G MANE Select	NP_004122.2:n.203+22A>G
NM_001346011.2:c.167+22A>G	NP_001332940.1:n.167+22A>G
NR_144343.2:n.233+22A>G