Canonical Allele Identifier: CA2124039577
Gene: GZMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24632802A= , CM000676.2:g.24632802A= GRCh38
NC_000014.8:g.25102008A= , CM000676.1:g.25102008A= GRCh37
NC_000014.7:g.24171848A= NCBI36
NG_028340.1:g.6425T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216341.9:c.203+113T= MANE Select ENSP00000216341.4:n.203+113T=
ENST00000216341.8:c.203+113T= ENSP00000216341.4:n.203+113T=
ENST00000382540.5:c.204-83T= ENSP00000371980.1:n.204-83T=
ENST00000382542.5:c.203+113T= ENSP00000371982.2:n.203+113T=
ENST00000415355.7:c.167+113T= ENSP00000387385.3:n.167+113T=
ENST00000526004.1:c.203+113T= ENSP00000434213.1:n.203+113T=
ENST00000530830.1:c.*126+113T= ENSP00000435084.1:n.*126+113T=
ENST00000532263.5:c.56-684T= ENSP00000432074.1:n.56-684T=
ENST00000554242.5:c.203+113T= ENSP00000450535.1:n.203+113T=
ENST00000616551.1:c.52-681T= ENSP00000479643.1:n.52-681T=
NM_004131.4:c.203+113T= NP_004122.2:n.203+113T=
XM_011536685.1:c.167+113T= XP_011534987.1:n.167+113T=
NM_001346011.1:c.167+113T= NP_001332940.1:n.167+113T=
NM_004131.5:c.203+113T= NP_004122.2:n.203+113T=
NR_144343.1:n.312+113T=
NM_004131.6:c.203+113T= MANE Select NP_004122.2:n.203+113T=
NM_001346011.2:c.167+113T= NP_001332940.1:n.167+113T=
NR_144343.2:n.233+113T=