Canonical Allele Identifier: CA324082818

Gene: RAC2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37236730T>G , CM000684.2:g.37236730T>G	GRCh38
NC_000022.10:g.37632770T>G , CM000684.1:g.37632770T>G	GRCh37
NC_000022.9:g.35962716T>G	NCBI36
NG_007288.1:g.12536A>C , LRG_97:g.12536A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699915.1:n.166-3812A>C
ENST00000249071.11:c.108-3812A>C MANE Select	ENSP00000249071.6:n.108-3812A>C
ENST00000249071.10:c.108-3812A>C	ENSP00000249071.6:n.108-3812A>C
ENST00000405484.5:c.87-3812A>C	ENSP00000385590.1:n.87-3812A>C
ENST00000406508.5:c.-25-3812A>C	ENSP00000385270.1:n.-25-3812A>C
ENST00000441619.5:c.108-3812A>C	ENSP00000403778.1:n.108-3812A>C
ENST00000469532.1:n.238-3812A>C
NM_002872.4:c.108-3812A>C	NP_002863.1:n.108-3812A>C
XM_006724286.2:c.108-3812A>C	XP_006724349.1:n.108-3812A>C
XM_006724286.3:c.108-3812A>C	XP_006724349.1:n.108-3812A>C
NM_002872.5:c.108-3812A>C MANE Select	NP_002863.1:n.108-3812A>C