Canonical Allele Identifier: CA450630870

Gene: RAB23

Linked Data

• MyVariant Identifiers: chr6:g.57055364A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.57190566A>C , CM000668.2:g.57190566A>C	GRCh38
NC_000006.11:g.57055364A>C , CM000668.1:g.57055364A>C	GRCh37
NC_000006.10:g.57163323A>C	NCBI36
NG_012170.1:g.36715T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000468148.6:c.609T>G MANE Select	ENSP00000417610.1:p.Gly203=
ENST00000317483.4:c.609T>G	ENSP00000320413.3:p.Gly203=
ENST00000468148.5:c.609T>G	ENSP00000417610.1:p.Gly203=
NM_001278666.1:c.609T>G	NP_001265595.1:p.Gly203=
NM_001278667.1:c.609T>G	NP_001265596.1:p.Gly203=
NM_001278668.1:c.609T>G	NP_001265597.1:p.Gly203=
NM_016277.4:c.609T>G	NP_057361.3:p.Gly203=
NM_183227.2:c.609T>G	NP_899050.1:p.Gly203=
NR_103822.1:n.468T>G
NM_016277.5:c.609T>G MANE Select	NP_057361.3:p.Gly203=
NM_001278666.2:c.609T>G	NP_001265595.1:p.Gly203=
NM_001278667.2:c.609T>G	NP_001265596.1:p.Gly203=
NM_001278668.2:c.609T>G	NP_001265597.1:p.Gly203=
NM_183227.3:c.609T>G	NP_899050.1:p.Gly203=
NR_103822.2:n.461T>G