Canonical Allele Identifier: CA1752546397
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs1801620327

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187312A>T , CM000669.2:g.151187312A>T GRCh38
NC_000007.13:g.150884399A>T , CM000669.1:g.150884399A>T GRCh37
NC_000007.12:g.150515332A>T NCBI36
NG_017016.1:g.5521T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-182T>A ENSP00000275838.1:n.-182T>A
ENST00000377867.7:c.271+140T>A ENSP00000367098.3:n.271+140T>A
ENST00000415615.1:c.*63T>A ENSP00000410871.1:n.*63T>A
NM_001142459.1:c.-182T>A NP_001135931.2:n.-182T>A
NM_001142460.1:c.-182T>A NP_001135932.2:n.-182T>A
NM_080871.3:c.271+140T>A NP_543147.2:n.271+140T>A
NM_080871.4:c.271+140T>A NP_543147.2:n.271+140T>A