Canonical Allele Identifier: CA118897
Gene: RAC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37232857C>T , CM000684.2:g.37232857C>T GRCh38
NC_000022.10:g.37628897C>T , CM000684.1:g.37628897C>T GRCh37
NC_000022.9:g.35958843C>T NCBI36
NG_007288.1:g.16409G>A , LRG_97:g.16409G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699915.1:n.227G>A
ENST00000249071.11:c.169G>A MANE Select ENSP00000249071.6:p.Asp57Asn
ENST00000249071.10:c.169G>A ENSP00000249071.6:p.Asp57Asn
ENST00000405484.5:c.148G>A ENSP00000385590.1:p.Asp50Asn
ENST00000406508.5:c.37G>A ENSP00000385270.1:p.Asp13Asn
ENST00000441619.5:c.169G>A ENSP00000403778.1:p.Asp57Asn
ENST00000469532.1:n.299G>A
NM_002872.4:c.169G>A NP_002863.1:p.Asp57Asn
XM_006724286.2:c.169G>A XP_006724349.1:p.Asp57Asn
XM_006724286.3:c.169G>A XP_006724349.1:p.Asp57Asn
NM_002872.5:c.169G>A MANE Select NP_002863.1:p.Asp57Asn
Search 100 bp 5'
Search 100 bp 3'