Canonical Allele Identifier: CA458881642
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs750676882
MyVariant Identifiers: chr7:g.150883666G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186579G>T , CM000669.2:g.151186579G>T GRCh38
NC_000007.13:g.150883666G>T , CM000669.1:g.150883666G>T GRCh37
NC_000007.12:g.150514599G>T NCBI36
NG_017016.1:g.6254C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.397C>A MANE Select ENSP00000391137.2:p.Arg133=
ENST00000275838.5:c.397C>A ENSP00000275838.1:p.Arg133=
ENST00000377867.7:c.352C>A ENSP00000367098.3:p.Arg118=
ENST00000420175.2:c.397C>A ENSP00000391137.2:p.Arg133=
NM_001142459.1:c.397C>A NP_001135931.2:p.Arg133=
NM_001142460.1:c.397C>A NP_001135932.2:p.Arg133=
NM_080871.3:c.352C>A NP_543147.2:p.Arg118=
XM_005249949.3:c.532C>A XP_005250006.1:p.Arg178=
NM_001142459.2:c.397C>A MANE Select NP_001135931.2:p.Arg133=
NM_080871.4:c.352C>A NP_543147.2:p.Arg118=