Canonical Allele Identifier: CA187670116

Gene: ARHGAP39

Linked Data

• dbSNP Id: rs969921010
• gnomAD v3: 8-144552651-G-C
• gnomAD v4: 8-144552651-G-C
• MyVariant Identifiers: chr8:g.145778035G>C (hg19) ; chr8:g.144552651G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144552651G>C , CM000670.2:g.144552651G>C	GRCh38
NC_000008.10:g.145778035G>C , CM000670.1:g.145778035G>C	GRCh37
NC_000008.9:g.145748843G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000377307.7:c.596+2909C>G MANE Select	ENSP00000366522.2:n.596+2909C>G
ENST00000276826.5:c.596+2909C>G	ENSP00000276826.5:n.596+2909C>G
ENST00000377307.6:c.596+2909C>G	ENSP00000366522.2:n.596+2909C>G
NM_001308207.1:c.596+2909C>G	NP_001295136.1:n.596+2909C>G
NM_001308208.1:c.596+2909C>G	NP_001295137.1:n.596+2909C>G
NM_025251.1:c.596+2909C>G	NP_079527.1:n.596+2909C>G
NM_025251.2:c.596+2909C>G	NP_079527.1:n.596+2909C>G
XM_011517308.1:c.596+2909C>G	XP_011515610.1:n.596+2909C>G
XM_011517309.1:c.596+2909C>G	XP_011515611.1:n.596+2909C>G
XM_011517311.1:c.164+2909C>G	XP_011515613.1:n.164+2909C>G
XM_011517312.1:c.125+2909C>G	XP_011515614.1:n.125+2909C>G
XM_011517309.2:c.596+2909C>G	XP_011515611.1:n.596+2909C>G
XM_011517312.2:c.125+2909C>G	XP_011515614.1:n.125+2909C>G
XM_017013870.2:c.596+2909C>G	XP_016869359.1:n.596+2909C>G
NM_001308208.2:c.596+2909C>G	NP_001295137.1:n.596+2909C>G
NM_025251.3:c.596+2909C>G MANE Select	NP_079527.1:n.596+2909C>G