Canonical Allele Identifier: CA169126483
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs957245156
gnomAD v4: 7-151187314-G-T
MyVariant Identifiers: chr7:g.150884401G>T (hg19) chr7:g.151187314G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187314G>T , CM000669.2:g.151187314G>T GRCh38
NC_000007.13:g.150884401G>T , CM000669.1:g.150884401G>T GRCh37
NC_000007.12:g.150515334G>T NCBI36
NG_017016.1:g.5519C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-184C>A ENSP00000275838.1:n.-184C>A
ENST00000377867.7:c.271+138C>A ENSP00000367098.3:n.271+138C>A
ENST00000415615.1:c.*61C>A ENSP00000410871.1:n.*61C>A
NM_001142459.1:c.-184C>A NP_001135931.2:n.-184C>A
NM_001142460.1:c.-184C>A NP_001135932.2:n.-184C>A
NM_080871.3:c.271+138C>A NP_543147.2:n.271+138C>A
NM_080871.4:c.271+138C>A NP_543147.2:n.271+138C>A
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