Canonical Allele Identifier: CA291147459

Gene: ARL17B LRRC37A

Linked Data

• dbSNP Id: rs936422411
• gnomAD v3: 17-46278324-T-C
• gnomAD v4: 17-46278324-T-C
• MyVariant Identifiers: chr17:g.44355690T>C (hg19) ; chr17:g.46278324T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46278324T>C , CM000679.2:g.46278324T>C	GRCh38
NC_000017.10:g.44355690T>C , CM000679.1:g.44355690T>C	GRCh37
NC_000017.9:g.41711467T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000705759.1:n.377-2906A>G (ARL17B)
ENST00000570618.5:c.*22-2906A>G (ARL17B)	ENSP00000459151.1:n.*22-2906A>G
XM_005256918.3:c.*22-2906A>G (ARL17B)	XP_005256975.1:n.*22-2906A>G
XM_005257887.3:c.27-21470T>C (LRRC37A)	XP_005257944.1:n.27-21470T>C
XM_011524162.1:c.*54-2906A>G (ARL17B)	XP_011522464.1:n.*54-2906A>G
XM_011525540.1:c.27-21470T>C (LRRC37A)	XP_011523842.1:n.27-21470T>C
NM_001103154.2:c.*22-2906A>G (ARL17B)	NP_001096624.1:n.*22-2906A>G
XM_011524162.3:c.*54-2906A>G (ARL17B)	XP_011522464.1:n.*54-2906A>G