Canonical Allele Identifier: CA2262235990
Gene: ARL17B HGNC NCBI
LRRC37A HGNC NCBI

Linked Data

dbSNP Id: rs2049648047

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46278287T>G , CM000679.2:g.46278287T>G GRCh38
NC_000017.10:g.44355653T>G , CM000679.1:g.44355653T>G GRCh37
NC_000017.9:g.41711430T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000705759.1:n.377-2869A>C (ARL17B)
ENST00000570618.5:c.*22-2869A>C (ARL17B) ENSP00000459151.1:n.*22-2869A>C
XM_005256918.3:c.*22-2869A>C (ARL17B) XP_005256975.1:n.*22-2869A>C
XM_005257887.3:c.27-21507T>G (LRRC37A) XP_005257944.1:n.27-21507T>G
XM_011524162.1:c.*54-2869A>C (ARL17B) XP_011522464.1:n.*54-2869A>C
XM_011525540.1:c.27-21507T>G (LRRC37A) XP_011523842.1:n.27-21507T>G
NM_001103154.2:c.*22-2869A>C (ARL17B) NP_001096624.1:n.*22-2869A>C
XM_011524162.3:c.*54-2869A>C (ARL17B) XP_011522464.1:n.*54-2869A>C