LDH info

Canonical Allele Identifier: CA15599071
Gene: ASTN2 HGNC NCBI
ASTN2-AS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs13290997

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.116551938A>G , CM000671.2:g.116551938A>G GRCh38
NC_000009.11:g.119314217A>G , CM000671.1:g.119314217A>G GRCh37
NC_000009.10:g.118354038A>G NCBI36
NG_021409.1:g.868101T>C
NG_021409.2:g.868120T>C

Transcript Alleles

HGVS Amino-acid change
NM_001184734.1:c.512-64438T>C (ASTN2) VV NP_001171663.1:p.=
NM_014010.4:c.3203-64438T>C (ASTN2) VV NP_054729.3:p.=
NM_198186.3:c.659-64438T>C (ASTN2) VV NP_937829.3:p.=
NM_198187.3:c.512-64438T>C (ASTN2) VV NP_937830.3:p.=
NM_198188.2:c.512-64438T>C (ASTN2) VV NP_937831.1:p.=
NR_033973.1:n.1325-172A>G (ASTN2-AS1)
NM_001365068.1:c.3356-64438T>C (ASTN2) VV NP_001351997.1:p.=
NM_001365069.1:c.3344-64438T>C (ASTN2) VV NP_001351998.1:p.=
NM_014010.5:c.3203-64438T>C (ASTN2) VV NP_054729.3:p.=
ENST00000288520.9:c.659-64438T>C ENSP00000288520.5:p.=
ENST00000313400.8:c.3356-64438T>C ENSP00000314038.4:p.=
ENST00000341734.8:c.512-64438T>C ENSP00000339925.4:p.=
ENST00000361209.6:c.3203-64438T>C ENSP00000354504.2:p.=
ENST00000361477.7:c.512-64438T>C ENSP00000355116.4:p.=
ENST00000373986.7:n.2525-64438T>C ENSP00000363098.3:p.=