Canonical Allele Identifier: CA291147588

Gene: ARL17B LRRC37A

Linked Data

• dbSNP Id: rs929740986
• MyVariant Identifiers: chr17:g.44355779T>G (hg19) ; chr17:g.46278413T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46278413T>G , CM000679.2:g.46278413T>G	GRCh38
NC_000017.10:g.44355779T>G , CM000679.1:g.44355779T>G	GRCh37
NC_000017.9:g.41711556T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705759.1:n.377-2995A>C (ARL17B)
ENST00000570618.5:c.*22-2995A>C (ARL17B)	ENSP00000459151.1:n.*22-2995A>C
XM_005256918.3:c.*22-2995A>C (ARL17B)	XP_005256975.1:n.*22-2995A>C
XM_005257887.3:c.27-21381T>G (LRRC37A)	XP_005257944.1:n.27-21381T>G
XM_011524162.1:c.*54-2995A>C (ARL17B)	XP_011522464.1:n.*54-2995A>C
XM_011525540.1:c.27-21381T>G (LRRC37A)	XP_011523842.1:n.27-21381T>G
NM_001103154.2:c.*22-2995A>C (ARL17B)	NP_001096624.1:n.*22-2995A>C
XM_011524162.3:c.*54-2995A>C (ARL17B)	XP_011522464.1:n.*54-2995A>C