Canonical Allele Identifier: CA2685657482
Gene: ASB10 HGNC NCBI

Linked Data

gnomAD v4: 7-151186362-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186362A>T , CM000669.2:g.151186362A>T GRCh38
NC_000007.13:g.150883449A>T , CM000669.1:g.150883449A>T GRCh37
NC_000007.12:g.150514382A>T NCBI36
NG_017016.1:g.6471T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.584+30T>A MANE Select ENSP00000391137.2:n.584+30T>A
ENST00000275838.5:c.584+30T>A ENSP00000275838.1:n.584+30T>A
ENST00000377867.7:c.539+30T>A ENSP00000367098.3:n.539+30T>A
ENST00000420175.2:c.584+30T>A ENSP00000391137.2:n.584+30T>A
NM_001142459.1:c.584+30T>A NP_001135931.2:n.584+30T>A
NM_001142460.1:c.584+30T>A NP_001135932.2:n.584+30T>A
NM_080871.3:c.539+30T>A NP_543147.2:n.539+30T>A
XM_005249949.3:c.719+30T>A XP_005250006.1:n.719+30T>A
NM_001142459.2:c.584+30T>A MANE Select NP_001135931.2:n.584+30T>A
NM_080871.4:c.539+30T>A NP_543147.2:n.539+30T>A
Search 100 bp 5'
Search 100 bp 3'