Canonical Allele Identifier: CA2624417487

Gene: GZMB

Linked Data

• gnomAD v4: 14-24632863-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632863G>T , CM000676.2:g.24632863G>T	GRCh38
NC_000014.8:g.25102069G>T , CM000676.1:g.25102069G>T	GRCh37
NC_000014.7:g.24171909G>T	NCBI36
NG_028340.1:g.6364C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216341.9:c.203+52C>A MANE Select	ENSP00000216341.4:n.203+52C>A
ENST00000216341.8:c.203+52C>A	ENSP00000216341.4:n.203+52C>A
ENST00000382540.5:c.203+52C>A	ENSP00000371980.1:n.203+52C>A
ENST00000382542.5:c.203+52C>A	ENSP00000371982.2:n.203+52C>A
ENST00000415355.7:c.167+52C>A	ENSP00000387385.3:n.167+52C>A
ENST00000526004.1:c.203+52C>A	ENSP00000434213.1:n.203+52C>A
ENST00000530830.1:c.*126+52C>A	ENSP00000435084.1:n.*126+52C>A
ENST00000532263.5:c.56-745C>A	ENSP00000432074.1:n.56-745C>A
ENST00000554242.5:c.203+52C>A	ENSP00000450535.1:n.203+52C>A
ENST00000616551.1:c.52-742C>A	ENSP00000479643.1:n.52-742C>A
NM_004131.4:c.203+52C>A	NP_004122.2:n.203+52C>A
XM_011536685.1:c.167+52C>A	XP_011534987.1:n.167+52C>A
NM_001346011.1:c.167+52C>A	NP_001332940.1:n.167+52C>A
NM_004131.5:c.203+52C>A	NP_004122.2:n.203+52C>A
NR_144343.1:n.312+52C>A
NM_004131.6:c.203+52C>A MANE Select	NP_004122.2:n.203+52C>A
NM_001346011.2:c.167+52C>A	NP_001332940.1:n.167+52C>A
NR_144343.2:n.233+52C>A