Canonical Allele Identifier: CA4573872

Gene: ASB10

Linked Data

• dbSNP Id: rs79026210
• ExAC: 7:150883582 T / C
• gnomAD v2: 7-150883582-T-C
• gnomAD v3: 7-151186495-T-C
• gnomAD v4: 7-151186495-T-C
• MyVariant Identifiers: chr7:g.150883582T>C (hg19) ; chr7:g.151186495T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186495T>C , CM000669.2:g.151186495T>C	GRCh38
NC_000007.13:g.150883582T>C , CM000669.1:g.150883582T>C	GRCh37
NC_000007.12:g.150514515T>C	NCBI36
NG_017016.1:g.6338A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.481A>G MANE Select	ENSP00000391137.2:p.Thr161Ala
ENST00000275838.5:c.481A>G	ENSP00000275838.1:p.Thr161Ala
ENST00000377867.7:c.436A>G	ENSP00000367098.3:p.Thr146Ala
ENST00000420175.2:c.481A>G	ENSP00000391137.2:p.Thr161Ala
NM_001142459.1:c.481A>G	NP_001135931.2:p.Thr161Ala
NM_001142460.1:c.481A>G	NP_001135932.2:p.Thr161Ala
NM_080871.3:c.436A>G	NP_543147.2:p.Thr146Ala
XM_005249949.3:c.616A>G	XP_005250006.1:p.Thr206Ala
NM_001142459.2:c.481A>G MANE Select	NP_001135931.2:p.Thr161Ala
NM_080871.4:c.436A>G	NP_543147.2:p.Thr146Ala