Canonical Allele Identifier: CA486768448

Linked Data

MyVariant Identifiers: chr14:g.68191934C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67725217C>G , CM000676.2:g.67725217C>G GRCh38
NC_000014.8:g.68191934C>G , CM000676.1:g.68191934C>G GRCh37
NC_000014.7:g.67261687C>G NCBI36
NG_008321.1:g.28332C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000551171.6:c.306C>G (RDH12) MANE Select ENSP00000449079.1:p.Thr102=
ENST00000267502.3:c.306C>G (RDH12) ENSP00000267502.3:p.Thr102=
ENST00000551171.5:c.306C>G (RDH12) ENSP00000449079.1:p.Thr102=
NM_152443.2:c.306C>G (RDH12) NP_689656.2:p.Thr102=
XM_017020925.2:c.1313-9978C>G (GPHN) XP_016876414.1:n.1313-9978C>G
NM_152443.3:c.306C>G (RDH12) MANE Select NP_689656.2:p.Thr102=