Canonical Allele Identifier: CA835247507
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs1438149641

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187344G>A , CM000669.2:g.151187344G>A GRCh38
NC_000007.13:g.150884431G>A , CM000669.1:g.150884431G>A GRCh37
NC_000007.12:g.150515364G>A NCBI36
NG_017016.1:g.5489C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-214C>T ENSP00000275838.1:n.-214C>T
ENST00000377867.7:c.271+108C>T ENSP00000367098.3:n.271+108C>T
ENST00000415615.1:c.*31C>T ENSP00000410871.1:n.*31C>T
NM_001142459.1:c.-214C>T NP_001135931.2:n.-214C>T
NM_001142460.1:c.-214C>T NP_001135932.2:n.-214C>T
NM_080871.3:c.271+108C>T NP_543147.2:n.271+108C>T
NM_080871.4:c.271+108C>T NP_543147.2:n.271+108C>T