LDH info

Canonical Allele Identifier: CA12266693
Gene: TAP2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4148871

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32835539A>G , CM000668.2:g.32835539A>G GRCh38
NC_000006.11:g.32803316A>G , CM000668.1:g.32803316A>G GRCh37
NC_000006.10:g.32911294A>G NCBI36
NG_009793.3:g.8232T>C

Transcript Alleles

HGVS Amino-acid change
NM_001290043.1:c.739+104T>C VV NP_001276972.1:p.=
NM_018833.2:c.739+104T>C VV NP_061313.2:p.=
NM_001290043.2:c.739+104T>C VV MANE Preferred NP_001276972.1:p.=
ENST00000374897.2:c.739+104T>C ENSP00000364032.2:p.=
ENST00000374899.8:c.739+104T>C ENSP00000364034.4:p.=
ENST00000452392.2:c.739+104T>C ENSP00000391806.2:p.=
ENST00000620123.4:c.739+104T>C ENSP00000481712.1:p.=