Canonical Allele Identifier: CA364625463

Gene: RAB23

Linked Data

• MyVariant Identifiers: chr6:g.57055371T>C (hg19) ; chr6:g.57190573T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.57190573T>C , CM000668.2:g.57190573T>C	GRCh38
NC_000006.11:g.57055371T>C , CM000668.1:g.57055371T>C	GRCh37
NC_000006.10:g.57163330T>C	NCBI36
NG_012170.1:g.36708A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000468148.6:c.602A>G MANE Select	ENSP00000417610.1:p.His201Arg
ENST00000317483.4:c.602A>G	ENSP00000320413.3:p.His201Arg
ENST00000468148.5:c.602A>G	ENSP00000417610.1:p.His201Arg
NM_001278666.1:c.602A>G	NP_001265595.1:p.His201Arg
NM_001278667.1:c.602A>G	NP_001265596.1:p.His201Arg
NM_001278668.1:c.602A>G	NP_001265597.1:p.His201Arg
NM_016277.4:c.602A>G	NP_057361.3:p.His201Arg
NM_183227.2:c.602A>G	NP_899050.1:p.His201Arg
NR_103822.1:n.461A>G
NM_016277.5:c.602A>G MANE Select	NP_057361.3:p.His201Arg
NM_001278666.2:c.602A>G	NP_001265595.1:p.His201Arg
NM_001278667.2:c.602A>G	NP_001265596.1:p.His201Arg
NM_001278668.2:c.602A>G	NP_001265597.1:p.His201Arg
NM_183227.3:c.602A>G	NP_899050.1:p.His201Arg
NR_103822.2:n.454A>G