Canonical Allele Identifier: CA389326602

Gene: GZMB

Linked Data

• MyVariant Identifiers: chr14:g.25102170A>C (hg19) ; chr14:g.24632964A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632964A>C , CM000676.2:g.24632964A>C	GRCh38
NC_000014.8:g.25102170A>C , CM000676.1:g.25102170A>C	GRCh37
NC_000014.7:g.24172010A>C	NCBI36
NG_028340.1:g.6263T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000216341.9:c.154T>G MANE Select	ENSP00000216341.4:p.Phe52Val
ENST00000216341.8:c.154T>G	ENSP00000216341.4:p.Phe52Val
ENST00000382540.5:c.154T>G	ENSP00000371980.1:p.Phe52Val
ENST00000382542.5:c.154T>G	ENSP00000371982.2:p.Phe52Val
ENST00000415355.7:c.118T>G	ENSP00000387385.3:p.Phe40Val
ENST00000526004.1:c.154T>G	ENSP00000434213.1:p.Phe52Val
ENST00000530830.1:c.*77T>G	ENSP00000435084.1:n.*77T>G
ENST00000532263.5:c.56-846T>G	ENSP00000432074.1:n.56-846T>G
ENST00000554242.5:c.154T>G	ENSP00000450535.1:p.Phe52Val
ENST00000616551.1:c.52-843T>G	ENSP00000479643.1:n.52-843T>G
NM_004131.4:c.154T>G	NP_004122.2:p.Phe52Val
XM_011536685.1:c.118T>G	XP_011534987.1:p.Phe40Val
NM_001346011.1:c.118T>G	NP_001332940.1:p.Phe40Val
NM_004131.5:c.154T>G	NP_004122.2:p.Phe52Val
NR_144343.1:n.263T>G
NM_004131.6:c.154T>G MANE Select	NP_004122.2:p.Phe52Val
NM_001346011.2:c.118T>G	NP_001332940.1:p.Phe40Val
NR_144343.2:n.184T>G