Canonical Allele Identifier: CA2675321741

Gene: SAR1B

Linked Data

• gnomAD v4: 5-134606930-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134606930G>A , CM000667.2:g.134606930G>A	GRCh38
NC_000005.9:g.133942620G>A , CM000667.1:g.133942620G>A	GRCh37
NC_000005.8:g.133970519G>A	NCBI36
NG_017002.1:g.30914C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000402673.7:c.*20C>T MANE Select	ENSP00000385432.2:n.*20C>T
ENST00000402673.6:c.*20C>T	ENSP00000385432.2:n.*20C>T
ENST00000439578.5:c.*20C>T	ENSP00000404997.1:n.*20C>T
ENST00000502539.5:c.*20C>T	ENSP00000426335.1:n.*20C>T
ENST00000507419.5:c.*20C>T	ENSP00000425339.1:n.*20C>T
ENST00000508363.5:n.2586C>T
NM_001033503.2:c.*20C>T	NP_001028675.1:n.*20C>T
NM_016103.3:c.*20C>T	NP_057187.1:n.*20C>T
NM_016103.4:c.*20C>T MANE Select	NP_057187.1:n.*20C>T
NM_001033503.3:c.*20C>T	NP_001028675.1:n.*20C>T