Canonical Allele Identifier: CA486768333

Linked Data

MyVariant Identifiers: chr14:g.68191832T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67725115T>A , CM000676.2:g.67725115T>A GRCh38
NC_000014.8:g.68191832T>A , CM000676.1:g.68191832T>A GRCh37
NC_000014.7:g.67261585T>A NCBI36
NG_008321.1:g.28230T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000551171.6:c.204T>A (RDH12) MANE Select ENSP00000449079.1:p.Ile68=
ENST00000267502.3:c.204T>A (RDH12) ENSP00000267502.3:p.Ile68=
ENST00000551171.5:c.204T>A (RDH12) ENSP00000449079.1:p.Ile68=
NM_152443.2:c.204T>A (RDH12) NP_689656.2:p.Ile68=
XM_017020925.2:c.1313-10080T>A (GPHN) XP_016876414.1:n.1313-10080T>A
NM_152443.3:c.204T>A (RDH12) MANE Select NP_689656.2:p.Ile68=