Canonical Allele Identifier: CA907987737

Gene: ARL8B

Linked Data

• dbSNP Id: rs1369887783
• MyVariant Identifiers: chr3:g.5188164G>A (hg19) ; chr3:g.5146479G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.5146479G>A , CM000665.2:g.5146479G>A	GRCh38
NC_000003.11:g.5188164G>A , CM000665.1:g.5188164G>A	GRCh37
NC_000003.10:g.5163164G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000256496.8:c.123+23891G>A MANE Select	ENSP00000256496.3:n.123+23891G>A
ENST00000256496.7:c.123+23891G>A	ENSP00000256496.3:n.123+23891G>A
ENST00000419534.2:c.123+23891G>A	ENSP00000402996.2:n.123+23891G>A
ENST00000429403.5:c.*111+17895G>A	ENSP00000405196.1:n.*111+17895G>A
ENST00000444332.1:n.297+23891G>A
ENST00000455168.5:c.295+23891G>A	ENSP00000400831.1:n.295+23891G>A
ENST00000611208.4:c.123+23891G>A	ENSP00000479202.1:n.123+23891G>A
NM_018184.2:c.123+23891G>A	NP_060654.1:n.123+23891G>A
XM_005265295.3:c.123+23891G>A	XP_005265352.1:n.123+23891G>A
NM_018184.3:c.123+23891G>A MANE Select	NP_060654.1:n.123+23891G>A