Canonical Allele Identifier: CA169126487
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs990100788
MyVariant Identifiers: chr7:g.150884416C>T (hg19) chr7:g.151187329C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187329C>T , CM000669.2:g.151187329C>T GRCh38
NC_000007.13:g.150884416C>T , CM000669.1:g.150884416C>T GRCh37
NC_000007.12:g.150515349C>T NCBI36
NG_017016.1:g.5504G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-199G>A ENSP00000275838.1:n.-199G>A
ENST00000377867.7:c.271+123G>A ENSP00000367098.3:n.271+123G>A
ENST00000415615.1:c.*46G>A ENSP00000410871.1:n.*46G>A
NM_001142459.1:c.-199G>A NP_001135931.2:n.-199G>A
NM_001142460.1:c.-199G>A NP_001135932.2:n.-199G>A
NM_080871.3:c.271+123G>A NP_543147.2:n.271+123G>A
NM_080871.4:c.271+123G>A NP_543147.2:n.271+123G>A
Search 100 bp 5'
Search 100 bp 3'