Canonical Allele Identifier: CA486768337

Linked Data

MyVariant Identifiers: chr14:g.68191835C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67725118C>T , CM000676.2:g.67725118C>T GRCh38
NC_000014.8:g.68191835C>T , CM000676.1:g.68191835C>T GRCh37
NC_000014.7:g.67261588C>T NCBI36
NG_008321.1:g.28233C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000551171.6:c.207C>T (RDH12) MANE Select ENSP00000449079.1:p.Ala69=
ENST00000267502.3:c.207C>T (RDH12) ENSP00000267502.3:p.Ala69=
ENST00000551171.5:c.207C>T (RDH12) ENSP00000449079.1:p.Ala69=
NM_152443.2:c.207C>T (RDH12) NP_689656.2:p.Ala69=
XM_017020925.2:c.1313-10077C>T (GPHN) XP_016876414.1:n.1313-10077C>T
NM_152443.3:c.207C>T (RDH12) MANE Select NP_689656.2:p.Ala69=