Canonical Allele Identifier: CA390148745
Gene: RDH12 HGNC NCBI
GPHN HGNC NCBI

Linked Data

gnomAD v4: 14-67725207-T-C
MyVariant Identifiers: chr14:g.68191924T>C (hg19) chr14:g.67725207T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67725207T>C , CM000676.2:g.67725207T>C GRCh38
NC_000014.8:g.68191924T>C , CM000676.1:g.68191924T>C GRCh37
NC_000014.7:g.67261677T>C NCBI36
NG_008321.1:g.28322T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000551171.6:c.296T>C (RDH12) MANE Select ENSP00000449079.1:p.Leu99Pro
ENST00000267502.3:c.296T>C (RDH12) ENSP00000267502.3:p.Leu99Pro
ENST00000551171.5:c.296T>C (RDH12) ENSP00000449079.1:p.Leu99Pro
NM_152443.2:c.296T>C (RDH12) NP_689656.2:p.Leu99Pro
XM_017020925.2:c.1313-9988T>C (GPHN) XP_016876414.1:n.1313-9988T>C
NM_152443.3:c.296T>C (RDH12) MANE Select NP_689656.2:p.Leu99Pro
Search 100 bp 5'
Search 100 bp 3'