LDH info

Canonical Allele Identifier: CA57549925
Gene: ACVR2A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1014064

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.147854585A>G , CM000664.2:g.147854585A>G GRCh38
NC_000002.11:g.148612154A>G , CM000664.1:g.148612154A>G GRCh37
NC_000002.10:g.148328624A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001278579.1:c.55+9378A>G VV NP_001265508.1:p.=
NM_001278580.1:c.-207+9879A>G VV NP_001265509.1:p.=
NM_001616.4:c.55+9378A>G VV NP_001607.1:p.=
XM_005263843.2:c.55+9378A>G XP_005263900.1:p.=
NM_001616.5:c.55+9378A>G VV MANE Preferred NP_001607.1:p.=
NM_001278579.2:c.55+9378A>G VV NP_001265508.1:p.=
ENST00000241416.11:c.55+9378A>G ENSP00000241416.7:p.=
ENST00000404590.1:c.55+9378A>G ENSP00000384338.1:p.=
ENST00000462659.1:n.183+9879A>G
ENST00000465329.1:n.179+9378A>G
ENST00000487959.5:n.190+9879A>G
ENST00000535787.5:c.-207+9879A>G ENSP00000439988.1:p.=