Canonical Allele Identifier: CA485677074

Gene: GZMB

Linked Data

• gnomAD v4: 14-24632961-G-A
• MyVariant Identifiers: chr14:g.25102167G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24632961G>A , CM000676.2:g.24632961G>A	GRCh38
NC_000014.8:g.25102167G>A , CM000676.1:g.25102167G>A	GRCh37
NC_000014.7:g.24172007G>A	NCBI36
NG_028340.1:g.6266C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216341.9:c.157C>T MANE Select	ENSP00000216341.4:p.Leu53=
ENST00000216341.8:c.157C>T	ENSP00000216341.4:p.Leu53=
ENST00000382540.5:c.157C>T	ENSP00000371980.1:p.Leu53=
ENST00000382542.5:c.157C>T	ENSP00000371982.2:p.Leu53=
ENST00000415355.7:c.121C>T	ENSP00000387385.3:p.Leu41=
ENST00000526004.1:c.157C>T	ENSP00000434213.1:p.Leu53=
ENST00000530830.1:c.*80C>T	ENSP00000435084.1:n.*80C>T
ENST00000532263.5:c.56-843C>T	ENSP00000432074.1:n.56-843C>T
ENST00000554242.5:c.157C>T	ENSP00000450535.1:p.Leu53=
ENST00000616551.1:c.52-840C>T	ENSP00000479643.1:n.52-840C>T
NM_004131.4:c.157C>T	NP_004122.2:p.Leu53=
XM_011536685.1:c.121C>T	XP_011534987.1:p.Leu41=
NM_001346011.1:c.121C>T	NP_001332940.1:p.Leu41=
NM_004131.5:c.157C>T	NP_004122.2:p.Leu53=
NR_144343.1:n.266C>T
NM_004131.6:c.157C>T MANE Select	NP_004122.2:p.Leu53=
NM_001346011.2:c.121C>T	NP_001332940.1:p.Leu41=
NR_144343.2:n.187C>T