Canonical Allele Identifier: CA1752546408
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs1801620488

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187315T>A , CM000669.2:g.151187315T>A GRCh38
NC_000007.13:g.150884402T>A , CM000669.1:g.150884402T>A GRCh37
NC_000007.12:g.150515335T>A NCBI36
NG_017016.1:g.5518A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-185A>T ENSP00000275838.1:n.-185A>T
ENST00000377867.7:c.271+137A>T ENSP00000367098.3:n.271+137A>T
ENST00000415615.1:c.*60A>T ENSP00000410871.1:n.*60A>T
NM_001142459.1:c.-185A>T NP_001135931.2:n.-185A>T
NM_001142460.1:c.-185A>T NP_001135932.2:n.-185A>T
NM_080871.3:c.271+137A>T NP_543147.2:n.271+137A>T
NM_080871.4:c.271+137A>T NP_543147.2:n.271+137A>T