Canonical Allele Identifier: CA485677058

Gene: GZMB

Linked Data

• MyVariant Identifiers: chr14:g.25102162T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632956T>G , CM000676.2:g.24632956T>G	GRCh38
NC_000014.8:g.25102162T>G , CM000676.1:g.25102162T>G	GRCh37
NC_000014.7:g.24172002T>G	NCBI36
NG_028340.1:g.6271A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000216341.9:c.162A>C MANE Select	ENSP00000216341.4:p.Ile54=
ENST00000216341.8:c.162A>C	ENSP00000216341.4:p.Ile54=
ENST00000382540.5:c.162A>C	ENSP00000371980.1:p.Ile54=
ENST00000382542.5:c.162A>C	ENSP00000371982.2:p.Ile54=
ENST00000415355.7:c.126A>C	ENSP00000387385.3:p.Ile42=
ENST00000526004.1:c.162A>C	ENSP00000434213.1:p.Ile54=
ENST00000530830.1:c.*85A>C	ENSP00000435084.1:n.*85A>C
ENST00000532263.5:c.56-838A>C	ENSP00000432074.1:n.56-838A>C
ENST00000554242.5:c.162A>C	ENSP00000450535.1:p.Ile54=
ENST00000616551.1:c.52-835A>C	ENSP00000479643.1:n.52-835A>C
NM_004131.4:c.162A>C	NP_004122.2:p.Ile54=
XM_011536685.1:c.126A>C	XP_011534987.1:p.Ile42=
NM_001346011.1:c.126A>C	NP_001332940.1:p.Ile42=
NM_004131.5:c.162A>C	NP_004122.2:p.Ile54=
NR_144343.1:n.271A>C
NM_004131.6:c.162A>C MANE Select	NP_004122.2:p.Ile54=
NM_001346011.2:c.126A>C	NP_001332940.1:p.Ile42=
NR_144343.2:n.192A>C