LDH info

Canonical Allele Identifier: CA2197918
Gene: PER2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2304672

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238277948G>C , CM000664.2:g.238277948G>C GRCh38
NC_000002.11:g.239186589G>C , CM000664.1:g.239186589G>C GRCh37
NC_000002.10:g.238851328G>C NCBI36
NG_012146.1:g.15619C>G

Transcript Alleles

HGVS Amino-acid change
NM_022817.2:c.-12C>G VV NP_073728.1:p.=
XM_005246111.3:c.-12C>G XP_005246168.1:p.=
XM_006712824.2:c.-12C>G XP_006712887.1:p.=
XM_005246111.4:c.-12C>G XP_005246168.1:p.=
XM_006712824.4:c.-12C>G XP_006712887.1:p.=
NM_022817.3:c.-12C>G VV MANE Preferred NP_073728.1:p.=
ENST00000254657.7:c.-12C>G ENSP00000254657.3:p.=
ENST00000431832.1:c.-12C>G ENSP00000405891.1:p.=