Canonical Allele Identifier: CA486768454

Linked Data

MyVariant Identifiers: chr14:g.68191937A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67725220A>G , CM000676.2:g.67725220A>G GRCh38
NC_000014.8:g.68191937A>G , CM000676.1:g.68191937A>G GRCh37
NC_000014.7:g.67261690A>G NCBI36
NG_008321.1:g.28335A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000551171.6:c.309A>G (RDH12) MANE Select ENSP00000449079.1:p.Lys103=
ENST00000267502.3:c.309A>G (RDH12) ENSP00000267502.3:p.Lys103=
ENST00000551171.5:c.309A>G (RDH12) ENSP00000449079.1:p.Lys103=
NM_152443.2:c.309A>G (RDH12) NP_689656.2:p.Lys103=
XM_017020925.2:c.1313-9975A>G (GPHN) XP_016876414.1:n.1313-9975A>G
NM_152443.3:c.309A>G (RDH12) MANE Select NP_689656.2:p.Lys103=