LDH info

Canonical Allele Identifier: CA10639566

Identifiers and link-outs to other resources

ClinVar Variation Id: 306335
ClinVar RCV Id: RCV000388699
dbSNP Id: rs713065

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86946478A>G , CM000673.2:g.86946478A>G GRCh38
NC_000011.9:g.86657520A>G , CM000673.1:g.86657520A>G GRCh37
NC_000011.8:g.86335168A>G NCBI36
NG_011752.1:g.13914T>C

Transcript Alleles

HGVS Amino-acid change
NM_012193.3:c.*4664T>C (FZD4) VV NP_036325.2:p.=
NR_120591.1:n.737-3878A>G (PRSS23)
NR_120592.1:n.630-4738A>G (PRSS23)
NR_120591.2:n.435-3878A>G (PRSS23)
NR_120592.2:n.328-4738A>G (PRSS23)
NM_012193.4:c.*4664T>C (FZD4) VV NP_036325.2:p.=
ENST00000528769.5:n.129-3878A>G
ENST00000531380.1:c.*4664T>C ENSP00000434034.1:p.=
ENST00000531521.1:n.243-3878A>G
ENST00000532234.5:c.*65-3878A>G ENSP00000436676.1:p.=
ENST00000533902.2:c.207-4738A>G ENSP00000437268.1:p.=