Canonical Allele Identifier: CA2144002677

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67725212G= , CM000676.2:g.67725212G= GRCh38
NC_000014.8:g.68191929G= , CM000676.1:g.68191929G= GRCh37
NC_000014.7:g.67261682G= NCBI36
NG_008321.1:g.28327G=

Transcript Alleles

HGVS Amino-acid change
ENST00000551171.6:c.301G= (RDH12) MANE Select ENSP00000449079.1:p.Asp101=
ENST00000267502.3:c.301G= (RDH12) ENSP00000267502.3:p.Asp101=
ENST00000551171.5:c.301G= (RDH12) ENSP00000449079.1:p.Asp101=
NM_152443.2:c.301G= (RDH12) NP_689656.2:p.Asp101=
XM_017020925.2:c.1313-9983G= (GPHN) XP_016876414.1:n.1313-9983G=
NM_152443.3:c.301G= (RDH12) MANE Select NP_689656.2:p.Asp101=