Canonical Allele Identifier: CA169126450
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs977066049
gnomAD v2: 7-150884372-G-A
gnomAD v4: 7-151187285-G-A
MyVariant Identifiers: chr7:g.150884372G>A (hg19) chr7:g.151187285G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187285G>A , CM000669.2:g.151187285G>A GRCh38
NC_000007.13:g.150884372G>A , CM000669.1:g.150884372G>A GRCh37
NC_000007.12:g.150515305G>A NCBI36
NG_017016.1:g.5548C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-155C>T ENSP00000275838.1:n.-155C>T
ENST00000377867.7:c.271+167C>T ENSP00000367098.3:n.271+167C>T
ENST00000415615.1:c.*90C>T ENSP00000410871.1:n.*90C>T
NM_001142459.1:c.-155C>T NP_001135931.2:n.-155C>T
NM_001142460.1:c.-155C>T NP_001135932.2:n.-155C>T
NM_080871.3:c.271+167C>T NP_543147.2:n.271+167C>T
NM_080871.4:c.271+167C>T NP_543147.2:n.271+167C>T
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