Canonical Allele Identifier: CA562819128

Gene: SAR1B

Linked Data

• dbSNP Id: rs1461572912
• gnomAD v2: 5-133942603-C-T
• gnomAD v4: 5-134606913-C-T
• MyVariant Identifiers: chr5:g.133942603C>T (hg19) ; chr5:g.134606913C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134606913C>T , CM000667.2:g.134606913C>T	GRCh38
NC_000005.9:g.133942603C>T , CM000667.1:g.133942603C>T	GRCh37
NC_000005.8:g.133970502C>T	NCBI36
NG_017002.1:g.30931G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000402673.7:c.*37G>A MANE Select	ENSP00000385432.2:n.*37G>A
ENST00000402673.6:c.*37G>A	ENSP00000385432.2:n.*37G>A
ENST00000439578.5:c.*37G>A	ENSP00000404997.1:n.*37G>A
ENST00000502539.5:c.*37G>A	ENSP00000426335.1:n.*37G>A
ENST00000507419.5:c.*37G>A	ENSP00000425339.1:n.*37G>A
ENST00000508363.5:n.2603G>A
NM_001033503.2:c.*37G>A	NP_001028675.1:n.*37G>A
NM_016103.3:c.*37G>A	NP_057187.1:n.*37G>A
NM_016103.4:c.*37G>A MANE Select	NP_057187.1:n.*37G>A
NM_001033503.3:c.*37G>A	NP_001028675.1:n.*37G>A