Canonical Allele Identifier: CA402583980
Gene: RAX HGNC NCBI

Linked Data

dbSNP Id: rs1603388768

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.59269146G>A , CM000680.2:g.59269146G>A GRCh38
NC_000018.9:g.56936378G>A , CM000680.1:g.56936378G>A GRCh37
NC_000018.8:g.55087358G>A NCBI36
NG_013031.1:g.9248C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000334889.4:c.899C>T MANE Select ENSP00000334813.3:p.Pro300Leu
ENST00000256852.7:c.*330C>T ENSP00000256852.7:n.*330C>T
ENST00000334889.3:c.899C>T ENSP00000334813.3:p.Pro300Leu
NM_013435.2:c.899C>T NP_038463.2:p.Pro300Leu
NM_013435.3:c.899C>T MANE Select NP_038463.2:p.Pro300Leu