Canonical Allele Identifier: CA2685657774
Gene: ASB10 HGNC NCBI

Linked Data

gnomAD v4: 7-151187356-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187356C>A , CM000669.2:g.151187356C>A GRCh38
NC_000007.13:g.150884443C>A , CM000669.1:g.150884443C>A GRCh37
NC_000007.12:g.150515376C>A NCBI36
NG_017016.1:g.5477G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-226G>T ENSP00000275838.1:n.-226G>T
ENST00000377867.7:c.271+96G>T ENSP00000367098.3:n.271+96G>T
ENST00000415615.1:c.*19G>T ENSP00000410871.1:n.*19G>T
NM_001142459.1:c.-226G>T NP_001135931.2:n.-226G>T
NM_001142460.1:c.-226G>T NP_001135932.2:n.-226G>T
NM_080871.3:c.271+96G>T NP_543147.2:n.271+96G>T
NM_080871.4:c.271+96G>T NP_543147.2:n.271+96G>T
Search 100 bp 5'
Search 100 bp 3'