Canonical Allele Identifier: CA10217688
Gene: RAC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37244098C>T , CM000684.2:g.37244098C>T GRCh38
NC_000022.10:g.37640138C>T , CM000684.1:g.37640138C>T GRCh37
NC_000022.9:g.35970084C>T NCBI36
NG_007288.1:g.5168G>A , LRG_97:g.5168G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699915.1:n.94-2440G>A
ENST00000249071.11:c.35+16G>A MANE Select ENSP00000249071.6:n.35+16G>A
ENST00000249071.10:c.35+16G>A ENSP00000249071.6:n.35+16G>A
ENST00000401529.3:c.35+16G>A ENSP00000385666.3:n.35+16G>A
ENST00000405484.5:c.14+37G>A ENSP00000385590.1:n.14+37G>A
ENST00000406508.5:c.-98+192G>A ENSP00000385270.1:n.-98+192G>A
ENST00000441619.5:c.35+16G>A ENSP00000403778.1:n.35+16G>A
ENST00000469532.1:n.165+16G>A
NM_002872.4:c.35+16G>A NP_002863.1:n.35+16G>A
XM_006724286.2:c.35+16G>A XP_006724349.1:n.35+16G>A
XM_006724286.3:c.35+16G>A XP_006724349.1:n.35+16G>A
NM_002872.5:c.35+16G>A MANE Select NP_002863.1:n.35+16G>A