Canonical Allele Identifier: CA704441137

Gene: GZMB

Linked Data

• dbSNP Id: rs753057742
• MyVariant Identifiers: chr14:g.25102088C>T (hg19) ; chr14:g.24632882C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632882C>T , CM000676.2:g.24632882C>T	GRCh38
NC_000014.8:g.25102088C>T , CM000676.1:g.25102088C>T	GRCh37
NC_000014.7:g.24171928C>T	NCBI36
NG_028340.1:g.6345G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216341.9:c.203+33G>A MANE Select	ENSP00000216341.4:n.203+33G>A
ENST00000216341.8:c.203+33G>A	ENSP00000216341.4:n.203+33G>A
ENST00000382540.5:c.203+33G>A	ENSP00000371980.1:n.203+33G>A
ENST00000382542.5:c.203+33G>A	ENSP00000371982.2:n.203+33G>A
ENST00000415355.7:c.167+33G>A	ENSP00000387385.3:n.167+33G>A
ENST00000526004.1:c.203+33G>A	ENSP00000434213.1:n.203+33G>A
ENST00000530830.1:c.*126+33G>A	ENSP00000435084.1:n.*126+33G>A
ENST00000532263.5:c.56-764G>A	ENSP00000432074.1:n.56-764G>A
ENST00000554242.5:c.203+33G>A	ENSP00000450535.1:n.203+33G>A
ENST00000616551.1:c.52-761G>A	ENSP00000479643.1:n.52-761G>A
NM_004131.4:c.203+33G>A	NP_004122.2:n.203+33G>A
XM_011536685.1:c.167+33G>A	XP_011534987.1:n.167+33G>A
NM_001346011.1:c.167+33G>A	NP_001332940.1:n.167+33G>A
NM_004131.5:c.203+33G>A	NP_004122.2:n.203+33G>A
NR_144343.1:n.312+33G>A
NM_004131.6:c.203+33G>A MANE Select	NP_004122.2:n.203+33G>A
NM_001346011.2:c.167+33G>A	NP_001332940.1:n.167+33G>A
NR_144343.2:n.233+33G>A