Canonical Allele Identifier: CA485677055

Gene: GZMB

Linked Data

• MyVariant Identifiers: chr14:g.25102161G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632955G>T , CM000676.2:g.24632955G>T	GRCh38
NC_000014.8:g.25102161G>T , CM000676.1:g.25102161G>T	GRCh37
NC_000014.7:g.24172001G>T	NCBI36
NG_028340.1:g.6272C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216341.9:c.163C>A MANE Select	ENSP00000216341.4:p.Arg55=
ENST00000216341.8:c.163C>A	ENSP00000216341.4:p.Arg55=
ENST00000382540.5:c.163C>A	ENSP00000371980.1:p.Arg55=
ENST00000382542.5:c.163C>A	ENSP00000371982.2:p.Arg55=
ENST00000415355.7:c.127C>A	ENSP00000387385.3:p.Arg43=
ENST00000526004.1:c.163C>A	ENSP00000434213.1:p.Arg55=
ENST00000530830.1:c.*86C>A	ENSP00000435084.1:n.*86C>A
ENST00000532263.5:c.56-837C>A	ENSP00000432074.1:n.56-837C>A
ENST00000554242.5:c.163C>A	ENSP00000450535.1:p.Arg55=
ENST00000616551.1:c.52-834C>A	ENSP00000479643.1:n.52-834C>A
NM_004131.4:c.163C>A	NP_004122.2:p.Arg55=
XM_011536685.1:c.127C>A	XP_011534987.1:p.Arg43=
NM_001346011.1:c.127C>A	NP_001332940.1:p.Arg43=
NM_004131.5:c.163C>A	NP_004122.2:p.Arg55=
NR_144343.1:n.272C>A
NM_004131.6:c.163C>A MANE Select	NP_004122.2:p.Arg55=
NM_001346011.2:c.127C>A	NP_001332940.1:p.Arg43=
NR_144343.2:n.193C>A