LDH info

Canonical Allele Identifier: CA14749823
Gene: SNAP25 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3746544

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10306436G>T , CM000682.2:g.10306436G>T GRCh38
NC_000020.10:g.10287084G>T , CM000682.1:g.10287084G>T GRCh37
NC_000020.9:g.10235084G>T NCBI36
NG_029626.1:g.92608G>T

Transcript Alleles

HGVS Amino-acid change
NM_003081.3:c.*239G>T VV NP_003072.2:p.=
NM_130811.2:c.*239G>T VV NP_570824.1:p.=
XM_005260808.3:c.*239G>T XP_005260865.1:p.=
XM_005260810.3:c.*239G>T XP_005260867.1:p.=
NM_001322902.1:c.*239G>T VV NP_001309831.1:p.=
NM_001322903.1:c.*239G>T VV NP_001309832.1:p.=
NM_001322904.1:c.*239G>T VV NP_001309833.1:p.=
NM_001322905.1:c.*239G>T VV NP_001309834.1:p.=
NM_001322906.1:c.*239G>T VV NP_001309835.1:p.=
NM_001322907.1:c.*239G>T VV NP_001309836.1:p.=
NM_001322908.1:c.*239G>T VV NP_001309837.1:p.=
NM_001322909.1:c.*239G>T VV NP_001309838.1:p.=
NM_001322910.1:c.*239G>T VV NP_001309839.1:p.=
NM_003081.4:c.*239G>T VV NP_003072.2:p.=
NM_130811.3:c.*239G>T VV NP_570824.1:p.=
XM_005260808.5:c.*239G>T XP_005260865.1:p.=
XM_017028021.2:c.*239G>T XP_016883510.1:p.=
XM_017028022.1:c.*239G>T XP_016883511.1:p.=
ENST00000254976.6:c.*239G>T ENSP00000254976.2:p.=
ENST00000304886.6:c.*239G>T ENSP00000307341.2:p.=
ENST00000495883.1:n.1274G>T