Canonical Allele Identifier: CA804207772

Gene: SAR1B

Linked Data

• dbSNP Id: rs1157899657
• gnomAD v3: 5-134606926-A-G
• gnomAD v4: 5-134606926-A-G
• MyVariant Identifiers: chr5:g.133942616A>G (hg19) ; chr5:g.134606926A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134606926A>G , CM000667.2:g.134606926A>G	GRCh38
NC_000005.9:g.133942616A>G , CM000667.1:g.133942616A>G	GRCh37
NC_000005.8:g.133970515A>G	NCBI36
NG_017002.1:g.30918T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000402673.7:c.*24T>C MANE Select	ENSP00000385432.2:n.*24T>C
ENST00000402673.6:c.*24T>C	ENSP00000385432.2:n.*24T>C
ENST00000439578.5:c.*24T>C	ENSP00000404997.1:n.*24T>C
ENST00000502539.5:c.*24T>C	ENSP00000426335.1:n.*24T>C
ENST00000507419.5:c.*24T>C	ENSP00000425339.1:n.*24T>C
ENST00000508363.5:n.2590T>C
NM_001033503.2:c.*24T>C	NP_001028675.1:n.*24T>C
NM_016103.3:c.*24T>C	NP_057187.1:n.*24T>C
NM_016103.4:c.*24T>C MANE Select	NP_057187.1:n.*24T>C
NM_001033503.3:c.*24T>C	NP_001028675.1:n.*24T>C