Canonical Allele Identifier: CA485677088

Gene: GZMB

Linked Data

• dbSNP Id: rs1294401278
• gnomAD v2: 14-25102171-G-A
• gnomAD v3: 14-24632965-G-A
• gnomAD v4: 14-24632965-G-A
• MyVariant Identifiers: chr14:g.25102171G>A (hg19) ; chr14:g.24632965G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632965G>A , CM000676.2:g.24632965G>A	GRCh38
NC_000014.8:g.25102171G>A , CM000676.1:g.25102171G>A	GRCh37
NC_000014.7:g.24172011G>A	NCBI36
NG_028340.1:g.6262C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216341.9:c.153C>T MANE Select	ENSP00000216341.4:p.Gly51=
ENST00000216341.8:c.153C>T	ENSP00000216341.4:p.Gly51=
ENST00000382540.5:c.153C>T	ENSP00000371980.1:p.Gly51=
ENST00000382542.5:c.153C>T	ENSP00000371982.2:p.Gly51=
ENST00000415355.7:c.117C>T	ENSP00000387385.3:p.Gly39=
ENST00000526004.1:c.153C>T	ENSP00000434213.1:p.Gly51=
ENST00000530830.1:c.*76C>T	ENSP00000435084.1:n.*76C>T
ENST00000532263.5:c.56-847C>T	ENSP00000432074.1:n.56-847C>T
ENST00000554242.5:c.153C>T	ENSP00000450535.1:p.Gly51=
ENST00000616551.1:c.52-844C>T	ENSP00000479643.1:n.52-844C>T
NM_004131.4:c.153C>T	NP_004122.2:p.Gly51=
XM_011536685.1:c.117C>T	XP_011534987.1:p.Gly39=
NM_001346011.1:c.117C>T	NP_001332940.1:p.Gly39=
NM_004131.5:c.153C>T	NP_004122.2:p.Gly51=
NR_144343.1:n.262C>T
NM_004131.6:c.153C>T MANE Select	NP_004122.2:p.Gly51=
NM_001346011.2:c.117C>T	NP_001332940.1:p.Gly39=
NR_144343.2:n.183C>T