Canonical Allele Identifier: CA390152908
Gene: RDH12 HGNC NCBI
ZFYVE26 HGNC NCBI
GPHN HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.68195936C>A (hg19) chr14:g.67729219C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67729219C>A , CM000676.2:g.67729219C>A GRCh38
NC_000014.8:g.68195936C>A , CM000676.1:g.68195936C>A GRCh37
NC_000014.7:g.67265689C>A NCBI36
NG_008321.1:g.32334C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551171.6:c.687C>A (RDH12) MANE Select ENSP00000449079.1:p.His229Gln
ENST00000267502.3:c.687C>A (RDH12) ENSP00000267502.3:p.His229Gln
ENST00000394455.6:n.3280G>T (ZFYVE26)
ENST00000551171.5:c.687C>A (RDH12) ENSP00000449079.1:p.His229Gln
ENST00000552873.1:n.56C>A (RDH12)
NM_152443.2:c.687C>A (RDH12) NP_689656.2:p.His229Gln
XM_017020925.2:c.1313-5976C>A (GPHN) XP_016876414.1:n.1313-5976C>A
XM_017021125.1:c.*523G>T (ZFYVE26) XP_016876614.1:n.*523G>T
NM_152443.3:c.687C>A (RDH12) MANE Select NP_689656.2:p.His229Gln
Search 100 bp 5'
Search 100 bp 3'