Canonical Allele Identifier: CA169126461
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs896059451
gnomAD v2: 7-150884383-C-T
gnomAD v3: 7-151187296-C-T
gnomAD v4: 7-151187296-C-T
MyVariant Identifiers: chr7:g.150884383C>T (hg19) chr7:g.151187296C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187296C>T , CM000669.2:g.151187296C>T GRCh38
NC_000007.13:g.150884383C>T , CM000669.1:g.150884383C>T GRCh37
NC_000007.12:g.150515316C>T NCBI36
NG_017016.1:g.5537G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-166G>A ENSP00000275838.1:n.-166G>A
ENST00000377867.7:c.271+156G>A ENSP00000367098.3:n.271+156G>A
ENST00000415615.1:c.*79G>A ENSP00000410871.1:n.*79G>A
NM_001142459.1:c.-166G>A NP_001135931.2:n.-166G>A
NM_001142460.1:c.-166G>A NP_001135932.2:n.-166G>A
NM_080871.3:c.271+156G>A NP_543147.2:n.271+156G>A
NM_080871.4:c.271+156G>A NP_543147.2:n.271+156G>A
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