Canonical Allele Identifier: CA2319043604
Gene: RAX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3770675C= , CM000681.2:g.3770675C= GRCh38
NC_000019.9:g.3770673C= , CM000681.1:g.3770673C= GRCh37
NC_000019.8:g.3721673C= NCBI36
NG_011565.1:g.6547G=

Transcript Alleles

HGVS Amino-acid change
ENST00000555633.3:c.501G= MANE Select ENSP00000450456.3:p.Arg167=
ENST00000555633.2:c.501G= ENSP00000450456.2:p.Arg167=
ENST00000555978.5:c.501G= ENSP00000450687.2:p.Arg167=
NM_032753.3:c.501G= NP_116142.1:p.Arg167=
XM_005259662.1:c.639G= XP_005259719.1:p.Arg213=
NM_001319074.1:c.639G= NP_001306003.1:p.Arg213=
NM_001319074.4:c.501G= MANE Select NP_001306003.2:p.Arg167=
NM_032753.4:c.501G= NP_116142.1:p.Arg167=