Canonical Allele Identifier: CA690144088

Gene: RDH5

Linked Data

• dbSNP Id: rs1474676164
• gnomAD v3: 12-55721515-G-C
• gnomAD v4: 12-55721515-G-C
• MyVariant Identifiers: chr12:g.56115299G>C (hg19) ; chr12:g.55721515G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721515G>C , CM000674.2:g.55721515G>C	GRCh38
NC_000012.11:g.56115299G>C , CM000674.1:g.56115299G>C	GRCh37
NC_000012.10:g.54401566G>C	NCBI36
NG_008606.1:g.6149G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.310+21G>C MANE Select	ENSP00000257895.6:n.310+21G>C
ENST00000257895.9:c.310+21G>C	ENSP00000257895.5:n.310+21G>C
ENST00000257899.3:c.326-174G>C
ENST00000547072.5:c.19+21G>C	ENSP00000449927.1:n.19+21G>C
ENST00000547301.1:n.245G>C
ENST00000548082.1:c.310+21G>C	ENSP00000447128.1:n.310+21G>C
ENST00000548123.1:c.300+21G>C
ENST00000548486.1:n.320+21G>C
ENST00000549424.1:c.118-174G>C	ENSP00000447621.1:n.118-174G>C
ENST00000550412.5:c.352-174G>C	ENSP00000447650.1:n.352-174G>C
ENST00000550608.1:n.449+21G>C
ENST00000551946.5:c.*114-174G>C	ENSP00000450201.1:n.*114-174G>C
ENST00000552930.5:c.19+21G>C	ENSP00000448014.1:n.19+21G>C
ENST00000553160.1:n.406-680G>C
ENST00000553187.5:n.320+21G>C
NM_001199771.1:c.310+21G>C	NP_001186700.1:n.310+21G>C
NM_002905.3:c.310+21G>C	NP_002896.2:n.310+21G>C
NR_037658.1:n.370-174G>C
NM_001199771.2:c.310+21G>C	NP_001186700.1:n.310+21G>C
NM_002905.5:c.310+21G>C MANE Select	NP_002896.2:n.310+21G>C
NM_001199771.3:c.310+21G>C	NP_001186700.1:n.310+21G>C