Canonical Allele Identifier: CA169126491
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs1036572644
gnomAD v3: 7-151187333-C-G
gnomAD v4: 7-151187333-C-G
MyVariant Identifiers: chr7:g.150884420C>G (hg19) chr7:g.151187333C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187333C>G , CM000669.2:g.151187333C>G GRCh38
NC_000007.13:g.150884420C>G , CM000669.1:g.150884420C>G GRCh37
NC_000007.12:g.150515353C>G NCBI36
NG_017016.1:g.5500G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-203G>C ENSP00000275838.1:n.-203G>C
ENST00000377867.7:c.271+119G>C ENSP00000367098.3:n.271+119G>C
ENST00000415615.1:c.*42G>C ENSP00000410871.1:n.*42G>C
NM_001142459.1:c.-203G>C NP_001135931.2:n.-203G>C
NM_001142460.1:c.-203G>C NP_001135932.2:n.-203G>C
NM_080871.3:c.271+119G>C NP_543147.2:n.271+119G>C
NM_080871.4:c.271+119G>C NP_543147.2:n.271+119G>C
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