LDH info

Canonical Allele Identifier: CA16106697
Gene: IL18RAP HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs917998

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102451696C>T , CM000664.2:g.102451696C>T GRCh38
NC_000002.11:g.103068156C>T , CM000664.1:g.103068156C>T GRCh37
NC_000002.10:g.102434588C>T NCBI36
NG_011481.1:g.37903C>T

Transcript Alleles

HGVS Amino-acid change
NM_003853.3:c.1385-70C>T VV NP_003844.1:p.=
XM_011512087.1:c.959-70C>T XP_011510389.1:p.=
XM_011512088.1:c.959-70C>T XP_011510390.1:p.=
XM_011512087.2:c.959-70C>T XP_011510389.1:p.=
XM_011512088.2:c.959-70C>T XP_011510390.1:p.=
XM_017005173.1:c.527-70C>T XP_016860662.1:p.=
XM_024453197.1:c.1385-70C>T XP_024308965.1:p.=
XM_024453198.1:c.1385-70C>T XP_024308966.1:p.=
XM_024453199.1:c.1385-70C>T XP_024308967.1:p.=
XM_024453200.1:c.1385-70C>T XP_024308968.1:p.=
XM_024453201.1:c.1385-70C>T XP_024308969.1:p.=
ENST00000264260.6:c.1385-70C>T ENSP00000264260.2:p.=
ENST00000409369.1:c.959-70C>T ENSP00000387201.1:p.=