Canonical Allele Identifier: CA293022
Gene: RAC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37241567A>G , CM000684.2:g.37241567A>G GRCh38
NC_000022.10:g.37637607A>G , CM000684.1:g.37637607A>G GRCh37
NC_000022.9:g.35967553A>G NCBI36
NG_007288.1:g.7699T>C , LRG_97:g.7699T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699915.1:n.165+20T>C
ENST00000249071.11:c.107+20T>C MANE Select ENSP00000249071.6:n.107+20T>C
ENST00000249071.10:c.107+20T>C ENSP00000249071.6:n.107+20T>C
ENST00000401529.3:c.107+20T>C ENSP00000385666.3:n.107+20T>C
ENST00000405484.5:c.86+20T>C ENSP00000385590.1:n.86+20T>C
ENST00000406508.5:c.-26+20T>C ENSP00000385270.1:n.-26+20T>C
ENST00000441619.5:c.107+20T>C ENSP00000403778.1:n.107+20T>C
ENST00000469532.1:n.237+20T>C
NM_002872.4:c.107+20T>C NP_002863.1:n.107+20T>C
XM_006724286.2:c.107+20T>C XP_006724349.1:n.107+20T>C
XM_006724286.3:c.107+20T>C XP_006724349.1:n.107+20T>C
NM_002872.5:c.107+20T>C MANE Select NP_002863.1:n.107+20T>C