Canonical Allele Identifier: CA150760

Gene: SERPINB7

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63798603G>A , CM000680.2:g.63798603G>A	GRCh38
NC_000018.9:g.61465837G>A , CM000680.1:g.61465837G>A	GRCh37
NC_000018.8:g.59616817G>A	NCBI36
NG_034150.1:g.50557G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398019.7:c.455-1G>A MANE Select	ENSP00000381101.2:n.455-1G>A
ENST00000336429.6:c.455-1G>A	ENSP00000337212.2:n.455-1G>A
ENST00000398019.6:c.455-1G>A	ENSP00000381101.2:n.455-1G>A
ENST00000447428.5:c.455-1G>A	ENSP00000402362.1:n.455-1G>A
ENST00000540675.5:c.404-1G>A	ENSP00000444572.1:n.404-1G>A
ENST00000546027.5:c.455-1G>A	ENSP00000444861.1:n.455-1G>A
NM_001040147.2:c.455-1G>A	NP_001035237.1:n.455-1G>A
NM_001261830.1:c.455-1G>A	NP_001248759.1:n.455-1G>A
NM_001261831.1:c.404-1G>A	NP_001248760.1:n.404-1G>A
NM_003784.3:c.455-1G>A	NP_003775.1:n.455-1G>A
XM_006722562.1:c.455-1G>A	XP_006722625.1:n.455-1G>A
XM_011526236.1:c.455-1G>A	XP_011524538.1:n.455-1G>A
XM_024451278.1:c.455-1G>A	XP_024307046.1:n.455-1G>A
NM_003784.4:c.455-1G>A MANE Select	NP_003775.1:n.455-1G>A
NM_001040147.3:c.455-1G>A	NP_001035237.1:n.455-1G>A
NM_001261830.2:c.455-1G>A	NP_001248759.1:n.455-1G>A
NM_001261831.2:c.404-1G>A	NP_001248760.1:n.404-1G>A