Canonical Allele Identifier: CA2319043603
Gene: RAX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3770672C= , CM000681.2:g.3770672C= GRCh38
NC_000019.9:g.3770670C= , CM000681.1:g.3770670C= GRCh37
NC_000019.8:g.3721670C= NCBI36
NG_011565.1:g.6550G=

Transcript Alleles

HGVS Amino-acid change
ENST00000555633.3:c.504G= MANE Select ENSP00000450456.3:p.Leu168=
ENST00000555633.2:c.504G= ENSP00000450456.2:p.Leu168=
ENST00000555978.5:c.504G= ENSP00000450687.2:p.Leu168=
NM_032753.3:c.504G= NP_116142.1:p.Leu168=
XM_005259662.1:c.642G= XP_005259719.1:p.Leu214=
NM_001319074.1:c.642G= NP_001306003.1:p.Leu214=
NM_001319074.4:c.504G= MANE Select NP_001306003.2:p.Leu168=
NM_032753.4:c.504G= NP_116142.1:p.Leu168=