Canonical Allele Identifier: CA4573855
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs768273821
ExAC: 7:150883495 C / T
gnomAD v2: 7-150883495-C-T
gnomAD v3: 7-151186408-C-T
gnomAD v4: 7-151186408-C-T
COSMIC: COSM6392426 COSM6392427 COSM6392428 COSM6392429
MyVariant Identifiers: chr7:g.150883495C>T (hg19) chr7:g.151186408C>T (hg38)
PubMed: PMID:28263302
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186408C>T , CM000669.2:g.151186408C>T GRCh38
NC_000007.13:g.150883495C>T , CM000669.1:g.150883495C>T GRCh37
NC_000007.12:g.150514428C>T NCBI36
NG_017016.1:g.6425G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.568G>A MANE Select ENSP00000391137.2:p.Gly190Arg
ENST00000275838.5:c.568G>A ENSP00000275838.1:p.Gly190Arg
ENST00000377867.7:c.523G>A ENSP00000367098.3:p.Gly175Arg
ENST00000420175.2:c.568G>A ENSP00000391137.2:p.Gly190Arg
NM_001142459.1:c.568G>A NP_001135931.2:p.Gly190Arg
NM_001142460.1:c.568G>A NP_001135932.2:p.Gly190Arg
NM_080871.3:c.523G>A NP_543147.2:p.Gly175Arg
XM_005249949.3:c.703G>A XP_005250006.1:p.Gly235Arg
NM_001142459.2:c.568G>A MANE Select NP_001135931.2:p.Gly190Arg
NM_080871.4:c.523G>A NP_543147.2:p.Gly175Arg
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