Canonical Allele Identifier: CA133647

Gene: SERPINB6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.2959279C>T , CM000668.2:g.2959279C>T	GRCh38
NC_000006.11:g.2959513C>T , CM000668.1:g.2959513C>T	GRCh37
NC_000006.10:g.2904512C>T	NCBI36
NG_027692.1:g.17887G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380520.6:c.54G>A	ENSP00000369891.1:p.Thr18=
ENST00000380539.7:c.54G>A MANE Select	ENSP00000369912.2:p.Thr18=
ENST00000612421.3:c.111G>A	ENSP00000484343.1:p.Thr37=
ENST00000616722.4:c.66G>A	ENSP00000481398.1:p.Thr22=
ENST00000642543.1:c.34-3609G>A	ENSP00000494161.1:n.34-3609G>A
ENST00000643098.1:c.54G>A	ENSP00000493936.1:p.Thr18=
ENST00000643227.1:c.54G>A	ENSP00000494217.1:p.Thr18=
ENST00000643314.1:n.2049G>A
ENST00000644178.1:c.54G>A	ENSP00000496073.1:p.Thr18=
ENST00000644388.1:c.54G>A	ENSP00000494650.1:p.Thr18=
ENST00000644693.1:c.54G>A	ENSP00000495361.1:p.Thr18=
ENST00000644777.1:c.54G>A	ENSP00000494783.1:p.Thr18=
ENST00000644828.1:c.4-3609G>A	ENSP00000495086.1:n.4-3609G>A
ENST00000645421.1:c.54G>A	ENSP00000496341.1:p.Thr18=
ENST00000645580.1:c.66G>A	ENSP00000495362.1:p.Thr22=
ENST00000646688.1:c.54G>A	ENSP00000494453.1:p.Thr18=
ENST00000646775.1:c.-102-3609G>A	ENSP00000496225.1:n.-102-3609G>A
ENST00000649845.1:c.*168G>A	ENSP00000497149.1:n.*168G>A
ENST00000335686.9:c.54G>A	ENSP00000338358.5:p.Thr18=
ENST00000380520.5:c.54G>A	ENSP00000369891.1:p.Thr18=
ENST00000380524.5:c.54G>A	ENSP00000369896.1:p.Thr18=
ENST00000380529.5:c.54G>A	ENSP00000369901.1:p.Thr18=
ENST00000380539.5:c.54G>A	ENSP00000369912.1:p.Thr18=
ENST00000380546.7:c.54G>A	ENSP00000369919.3:p.Thr18=
ENST00000612421.2:c.111G>A	ENSP00000484343.1:p.Thr37=
ENST00000616722.3:c.66G>A	ENSP00000481398.1:p.Thr22=
NM_001195291.2:c.66G>A	NP_001182220.2:p.Thr22=
NM_001271822.1:c.96G>A	NP_001258751.1:p.Thr32=
NM_001271823.1:c.111G>A	NP_001258752.1:p.Thr37=
NM_001271824.1:c.54G>A	NP_001258753.1:p.Thr18=
NM_001271825.1:c.54G>A	NP_001258754.1:p.Thr18=
NM_001297699.1:c.54G>A	NP_001284628.1:p.Thr18=
NM_001297700.1:c.54G>A	NP_001284629.1:p.Thr18=
NM_004568.5:c.54G>A	NP_004559.4:p.Thr18=
XM_011514672.1:c.288G>A	XP_011512974.1:p.Thr96=
XM_011514673.1:c.54G>A	XP_011512975.1:p.Thr18=
XM_011514674.1:c.54G>A	XP_011512976.1:p.Thr18=
XM_011514675.1:c.34-3609G>A	XP_011512977.1:n.34-3609G>A
XM_011514676.1:c.34-3609G>A	XP_011512978.1:n.34-3609G>A
XM_011514674.2:c.54G>A	XP_011512976.1:p.Thr18=
XM_011514676.2:c.34-3609G>A	XP_011512978.1:n.34-3609G>A
XM_017010940.1:c.66G>A	XP_016866429.1:p.Thr22=
XM_017010941.1:c.34-3609G>A	XP_016866430.1:n.34-3609G>A
XM_024446462.1:c.66G>A	XP_024302230.1:p.Thr22=
XM_024446463.1:c.66G>A	XP_024302231.1:p.Thr22=
XM_024446464.1:c.54G>A	XP_024302232.1:p.Thr18=
XM_024446465.1:c.34-3609G>A	XP_024302233.1:n.34-3609G>A
NM_001195291.3:c.66G>A	NP_001182220.2:p.Thr22=
NM_001271822.2:c.96G>A	NP_001258751.1:p.Thr32=
NM_001271823.2:c.111G>A	NP_001258752.1:p.Thr37=
NM_001271824.2:c.54G>A	NP_001258753.1:p.Thr18=
NM_001271825.2:c.54G>A	NP_001258754.1:p.Thr18=
NM_001297699.2:c.54G>A	NP_001284628.1:p.Thr18=
NM_001297700.2:c.54G>A	NP_001284629.1:p.Thr18=
NM_001374515.1:c.66G>A	NP_001361444.1:p.Thr22=
NM_001374516.1:c.54G>A	NP_001361445.1:p.Thr18=
NM_001374517.1:c.34-3609G>A	NP_001361446.1:n.34-3609G>A
NM_004568.6:c.54G>A MANE Select	NP_004559.4:p.Thr18=
NR_164657.1:n.99G>A