LDH info

Canonical Allele Identifier: CA15182751
Gene: ITGA6 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12621278

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.172446825A>G , CM000664.2:g.172446825A>G GRCh38
NC_000002.11:g.173311553A>G , CM000664.1:g.173311553A>G GRCh37
NC_000002.10:g.173019799A>G NCBI36
NG_008853.1:g.24240A>G

Transcript Alleles

HGVS Amino-acid change
NM_000210.2:c.183-18714A>G VV NP_000201.2:p.=
NM_000210.3:c.183-18714A>G VV NP_000201.2:p.=
NM_001079818.1:c.183-18714A>G VV NP_001073286.1:p.=
NM_001079818.2:c.183-18714A>G VV NP_001073286.1:p.=
NM_001316306.1:c.-160-18714A>G VV NP_001303235.1:p.=
XM_006712510.1:c.183-18714A>G XP_006712573.1:p.=
XM_006712511.1:c.183-18714A>G XP_006712574.1:p.=
NM_001365529.1:c.183-18714A>G VV NP_001352458.1:p.=
NM_001365530.1:c.183-18714A>G VV NP_001352459.1:p.=
XM_017004005.1:c.-160-18714A>G XP_016859494.1:p.=
XM_017004006.1:c.-160-18714A>G XP_016859495.1:p.=
XM_017004007.1:c.-160-18714A>G XP_016859496.1:p.=
XM_017004008.1:c.-160-18714A>G XP_016859497.1:p.=
NM_001079818.3:c.183-18714A>G VV MANE Preferred NP_001073286.1:p.=
NM_000210.4:c.183-18714A>G VV NP_000201.2:p.=
NM_001316306.2:c.-160-18714A>G VV NP_001303235.1:p.=
NM_001365529.2:c.183-18714A>G VV NP_001352458.1:p.=
NM_001365530.2:c.183-18714A>G VV NP_001352459.1:p.=
ENST00000264107.11:c.183-18714A>G ENSP00000264107.7:p.=
ENST00000409080.5:n.183-18714A>G ENSP00000386896.1:p.=
ENST00000409532.5:c.-160-18714A>G ENSP00000386614.1:p.=
ENST00000412899.5:c.-160-18714A>G ENSP00000413470.1:p.=
ENST00000442250.5:n.183-18714A>G ENSP00000406694.1:p.=
ENST00000458358.5:n.183-18714A>G ENSP00000394169.1:p.=