Canonical Allele Identifier: CA2124039571
Gene: GZMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24632786C= , CM000676.2:g.24632786C= GRCh38
NC_000014.8:g.25101992C= , CM000676.1:g.25101992C= GRCh37
NC_000014.7:g.24171832C= NCBI36
NG_028340.1:g.6441G=

Transcript Alleles

HGVS Amino-acid change
ENST00000216341.9:c.203+129G= MANE Select ENSP00000216341.4:n.203+129G=
ENST00000216341.8:c.203+129G= ENSP00000216341.4:n.203+129G=
ENST00000382540.5:c.204-67G= ENSP00000371980.1:n.204-67G=
ENST00000382542.5:c.203+129G= ENSP00000371982.2:n.203+129G=
ENST00000415355.7:c.167+129G= ENSP00000387385.3:n.167+129G=
ENST00000526004.1:c.203+129G= ENSP00000434213.1:n.203+129G=
ENST00000530830.1:c.*126+129G= ENSP00000435084.1:n.*126+129G=
ENST00000532263.5:c.56-668G= ENSP00000432074.1:n.56-668G=
ENST00000554242.5:c.203+129G= ENSP00000450535.1:n.203+129G=
ENST00000616551.1:c.52-665G= ENSP00000479643.1:n.52-665G=
NM_004131.4:c.203+129G= NP_004122.2:n.203+129G=
XM_011536685.1:c.167+129G= XP_011534987.1:n.167+129G=
NM_001346011.1:c.167+129G= NP_001332940.1:n.167+129G=
NM_004131.5:c.203+129G= NP_004122.2:n.203+129G=
NR_144343.1:n.312+129G=
NM_004131.6:c.203+129G= MANE Select NP_004122.2:n.203+129G=
NM_001346011.2:c.167+129G= NP_001332940.1:n.167+129G=
NR_144343.2:n.233+129G=