Canonical Allele Identifier: CA2124039678

Gene: GZMB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632962G= , CM000676.2:g.24632962G=	GRCh38
NC_000014.8:g.25102168G= , CM000676.1:g.25102168G=	GRCh37
NC_000014.7:g.24172008G=	NCBI36
NG_028340.1:g.6265C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216341.9:c.156C= MANE Select	ENSP00000216341.4:p.Phe52=
ENST00000216341.8:c.156C=	ENSP00000216341.4:p.Phe52=
ENST00000382540.5:c.156C=	ENSP00000371980.1:p.Phe52=
ENST00000382542.5:c.156C=	ENSP00000371982.2:p.Phe52=
ENST00000415355.7:c.120C=	ENSP00000387385.3:p.Phe40=
ENST00000526004.1:c.156C=	ENSP00000434213.1:p.Phe52=
ENST00000530830.1:c.*79C=	ENSP00000435084.1:n.*79C=
ENST00000532263.5:c.56-844C=	ENSP00000432074.1:n.56-844C=
ENST00000554242.5:c.156C=	ENSP00000450535.1:p.Phe52=
ENST00000616551.1:c.52-841C=	ENSP00000479643.1:n.52-841C=
NM_004131.4:c.156C=	NP_004122.2:p.Phe52=
XM_011536685.1:c.120C=	XP_011534987.1:p.Phe40=
NM_001346011.1:c.120C=	NP_001332940.1:p.Phe40=
NM_004131.5:c.156C=	NP_004122.2:p.Phe52=
NR_144343.1:n.265C=
NM_004131.6:c.156C= MANE Select	NP_004122.2:p.Phe52=
NM_001346011.2:c.120C=	NP_001332940.1:p.Phe40=
NR_144343.2:n.186C=