Canonical Allele Identifier: CA835247501
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs1290655358
gnomAD v4: 7-151187324-T-C
MyVariant Identifiers: chr7:g.150884411T>C (hg19) chr7:g.151187324T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187324T>C , CM000669.2:g.151187324T>C GRCh38
NC_000007.13:g.150884411T>C , CM000669.1:g.150884411T>C GRCh37
NC_000007.12:g.150515344T>C NCBI36
NG_017016.1:g.5509A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-194A>G ENSP00000275838.1:n.-194A>G
ENST00000377867.7:c.271+128A>G ENSP00000367098.3:n.271+128A>G
ENST00000415615.1:c.*51A>G ENSP00000410871.1:n.*51A>G
NM_001142459.1:c.-194A>G NP_001135931.2:n.-194A>G
NM_001142460.1:c.-194A>G NP_001135932.2:n.-194A>G
NM_080871.3:c.271+128A>G NP_543147.2:n.271+128A>G
NM_080871.4:c.271+128A>G NP_543147.2:n.271+128A>G
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