Canonical Allele Identifier: CA4574038
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs772042771
ExAC: 7:150884365 A / G
gnomAD v2: 7-150884365-A-G
gnomAD v4: 7-151187278-A-G
MyVariant Identifiers: chr7:g.150884365A>G (hg19) chr7:g.151187278A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187278A>G , CM000669.2:g.151187278A>G GRCh38
NC_000007.13:g.150884365A>G , CM000669.1:g.150884365A>G GRCh37
NC_000007.12:g.150515298A>G NCBI36
NG_017016.1:g.5555T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-148T>C ENSP00000275838.1:n.-148T>C
ENST00000377867.7:c.271+174T>C ENSP00000367098.3:n.271+174T>C
ENST00000415615.1:c.*97T>C ENSP00000410871.1:n.*97T>C
NM_001142459.1:c.-148T>C NP_001135931.2:n.-148T>C
NM_001142460.1:c.-148T>C NP_001135932.2:n.-148T>C
NM_080871.3:c.271+174T>C NP_543147.2:n.271+174T>C
NM_080871.4:c.271+174T>C NP_543147.2:n.271+174T>C
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