Canonical Allele Identifier: CA2466152360
Gene: NSDHL HGNC NCBI

Linked Data

dbSNP Id: rs1933544301

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.152862537T>G , CM000685.2:g.152862537T>G GRCh38
NC_000023.10:g.152031081T>G , CM000685.1:g.152031081T>G GRCh37
NC_000023.9:g.151781737T>G NCBI36
NG_009163.1:g.36571T>G
NG_009163.2:g.36571T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370274.8:c.415-59T>G MANE Select ENSP00000359297.3:n.415-59T>G
ENST00000370274.7:c.415-59T>G ENSP00000359297.3:n.415-59T>G
ENST00000432467.1:c.415-59T>G ENSP00000396266.1:n.415-59T>G
ENST00000440023.5:c.415-59T>G ENSP00000391854.1:n.415-59T>G
NM_001129765.1:c.415-59T>G NP_001123237.1:n.415-59T>G
NM_015922.2:c.415-59T>G NP_057006.1:n.415-59T>G
XM_011531178.1:c.415-59T>G XP_011529480.1:n.415-59T>G
XM_011531178.2:c.415-59T>G XP_011529480.1:n.415-59T>G
XM_017029564.1:c.463-59T>G XP_016885053.1:n.463-59T>G
NM_015922.3:c.415-59T>G MANE Select NP_057006.1:n.415-59T>G
NM_001129765.2:c.415-59T>G NP_001123237.1:n.415-59T>G