Canonical Allele Identifier: CA486768437

Linked Data

MyVariant Identifiers: chr14:g.68191925A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67725208A>T , CM000676.2:g.67725208A>T GRCh38
NC_000014.8:g.68191925A>T , CM000676.1:g.68191925A>T GRCh37
NC_000014.7:g.67261678A>T NCBI36
NG_008321.1:g.28323A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000551171.6:c.297A>T (RDH12) MANE Select ENSP00000449079.1:p.Leu99=
ENST00000267502.3:c.297A>T (RDH12) ENSP00000267502.3:p.Leu99=
ENST00000551171.5:c.297A>T (RDH12) ENSP00000449079.1:p.Leu99=
NM_152443.2:c.297A>T (RDH12) NP_689656.2:p.Leu99=
XM_017020925.2:c.1313-9987A>T (GPHN) XP_016876414.1:n.1313-9987A>T
NM_152443.3:c.297A>T (RDH12) MANE Select NP_689656.2:p.Leu99=