Canonical Allele Identifier: CA2675321714

Gene: SAR1B

Linked Data

• gnomAD v4: 5-134606854-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134606854C>A , CM000667.2:g.134606854C>A	GRCh38
NC_000005.9:g.133942544C>A , CM000667.1:g.133942544C>A	GRCh37
NC_000005.8:g.133970443C>A	NCBI36
NG_017002.1:g.30990G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402673.7:c.*96G>T MANE Select	ENSP00000385432.2:n.*96G>T
ENST00000402673.6:c.*96G>T	ENSP00000385432.2:n.*96G>T
ENST00000439578.5:c.*96G>T	ENSP00000404997.1:n.*96G>T
ENST00000502539.5:c.*96G>T	ENSP00000426335.1:n.*96G>T
ENST00000507419.5:c.*96G>T	ENSP00000425339.1:n.*96G>T
ENST00000508363.5:n.2662G>T
NM_001033503.2:c.*96G>T	NP_001028675.1:n.*96G>T
NM_016103.3:c.*96G>T	NP_057187.1:n.*96G>T
NM_016103.4:c.*96G>T MANE Select	NP_057187.1:n.*96G>T
NM_001033503.3:c.*96G>T	NP_001028675.1:n.*96G>T