Canonical Allele Identifier: CA2625366122

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67729161C>A , CM000676.2:g.67729161C>A GRCh38
NC_000014.8:g.68195878C>A , CM000676.1:g.68195878C>A GRCh37
NC_000014.7:g.67265631C>A NCBI36
NG_008321.1:g.32276C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551171.6:c.659-30C>A (RDH12) MANE Select ENSP00000449079.1:n.659-30C>A
ENST00000267502.3:c.659-30C>A (RDH12) ENSP00000267502.3:n.659-30C>A
ENST00000394455.6:n.3288+50G>T (ZFYVE26)
ENST00000551171.5:c.659-30C>A (RDH12) ENSP00000449079.1:n.659-30C>A
ENST00000552873.1:n.28-30C>A (RDH12)
NM_152443.2:c.659-30C>A (RDH12) NP_689656.2:n.659-30C>A
XM_017020925.2:c.1313-6034C>A (GPHN) XP_016876414.1:n.1313-6034C>A
XM_017021125.1:c.*581G>T (ZFYVE26) XP_016876614.1:n.*581G>T
NM_152443.3:c.659-30C>A (RDH12) MANE Select NP_689656.2:n.659-30C>A