Canonical Allele Identifier: CA7139926
Gene: GZMB HGNC NCBI

Linked Data

dbSNP Id: rs8192917

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000216341.9:c.164G>A MANE Select ENSP00000216341.4:p.Arg55Gln
ENST00000216341.8:c.164G>A ENSP00000216341.4:p.Arg55Gln
ENST00000382540.5:c.164G>A ENSP00000371980.1:p.Arg55Gln
ENST00000382542.5:n.164G>A ENSP00000371982.2:p.Arg55Gln
ENST00000415355.7:c.128G>A ENSP00000387385.3:p.Arg43Gln
ENST00000526004.1:c.164G>A ENSP00000434213.1:p.Arg55Gln
ENST00000530830.1:c.*87G>A ENSP00000435084.1:n.*87G>A
ENST00000532263.5:n.56-836G>A ENSP00000432074.1:n.56-836G>A
ENST00000554242.5:n.164G>A ENSP00000450535.1:p.Arg55Gln
ENST00000616551.1:n.52-833G>A ENSP00000479643.1:n.52-833G>A
NM_004131.4:c.164G>A NP_004122.2:p.Arg55Gln
XM_011536685.1:c.128G>A XP_011534987.1:p.Arg43Gln
NM_001346011.1:c.128G>A NP_001332940.1:p.Arg43Gln
NM_004131.5:c.164G>A NP_004122.2:p.Arg55Gln
NR_144343.1:n.273G>A
NM_004131.6:c.164G>A MANE Select NP_004122.2:p.Arg55Gln
NM_001346011.2:c.128G>A NP_001332940.1:p.Arg43Gln
NR_144343.2:n.194G>A