Canonical Allele Identifier: CA169126427
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs1055906214
gnomAD v3: 7-151187269-G-T
gnomAD v4: 7-151187269-G-T
MyVariant Identifiers: chr7:g.150884356G>T (hg19) chr7:g.151187269G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187269G>T , CM000669.2:g.151187269G>T GRCh38
NC_000007.13:g.150884356G>T , CM000669.1:g.150884356G>T GRCh37
NC_000007.12:g.150515289G>T NCBI36
NG_017016.1:g.5564C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-139C>A ENSP00000275838.1:n.-139C>A
ENST00000377867.7:c.271+183C>A ENSP00000367098.3:n.271+183C>A
ENST00000415615.1:c.*106C>A ENSP00000410871.1:n.*106C>A
NM_001142459.1:c.-139C>A NP_001135931.2:n.-139C>A
NM_001142460.1:c.-139C>A NP_001135932.2:n.-139C>A
NM_080871.3:c.271+183C>A NP_543147.2:n.271+183C>A
NM_080871.4:c.271+183C>A NP_543147.2:n.271+183C>A
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