Canonical Allele Identifier: CA365829816

Gene: ARHGAP18

Linked Data

• MyVariant Identifiers: chr6:g.130031188C>G (hg19) ; chr6:g.129710043C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129710043C>G , CM000668.2:g.129710043C>G	GRCh38
NC_000006.11:g.130031188C>G , CM000668.1:g.130031188C>G	GRCh37
NC_000006.10:g.130072881C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368149.3:c.94G>C MANE Select	ENSP00000357131.2:p.Gly32Arg
ENST00000368149.2:c.94G>C	ENSP00000357131.2:p.Gly32Arg
NM_033515.2:c.94G>C	NP_277050.2:p.Gly32Arg
XM_005267213.1:c.94G>C	XP_005267270.1:p.Gly32Arg
NM_033515.3:c.94G>C MANE Select	NP_277050.2:p.Gly32Arg