Canonical Allele Identifier: CA389326564

Gene: GZMB

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632954C>G , CM000676.2:g.24632954C>G	GRCh38
NC_000014.8:g.25102160C>G , CM000676.1:g.25102160C>G	GRCh37
NC_000014.7:g.24172000C>G	NCBI36
NG_028340.1:g.6273G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004131.6:c.164G>C MANE Select	NP_004122.2:p.Arg55Pro
ENST00000216341.9:c.164G>C MANE Select	ENSP00000216341.4:p.Arg55Pro
NM_001346011.1:c.128G>C	NP_001332940.1:p.Arg43Pro
NM_001346011.2:c.128G>C	NP_001332940.1:p.Arg43Pro
NM_004131.4:c.164G>C	NP_004122.2:p.Arg55Pro
NM_004131.5:c.164G>C	NP_004122.2:p.Arg55Pro
NR_144343.1:n.273G>C
NR_144343.2:n.194G>C
ENST00000216341.8:c.164G>C	ENSP00000216341.4:p.Arg55Pro
ENST00000382540.5:c.164G>C	ENSP00000371980.1:p.Arg55Pro
ENST00000382542.5:c.164G>C	ENSP00000371982.2:p.Arg55Pro
ENST00000415355.7:c.128G>C	ENSP00000387385.3:p.Arg43Pro
ENST00000526004.1:c.164G>C	ENSP00000434213.1:p.Arg55Pro
ENST00000530830.1:c.*87G>C	ENSP00000435084.1:n.*87G>C
ENST00000532263.5:c.56-836G>C	ENSP00000432074.1:n.56-836G>C
ENST00000554242.5:c.164G>C	ENSP00000450535.1:p.Arg55Pro
ENST00000616551.1:c.52-833G>C	ENSP00000479643.1:n.52-833G>C
XM_011536685.1:c.128G>C	XP_011534987.1:p.Arg43Pro