Canonical Allele Identifier: CA169126529

Gene: ASB10

Linked Data

• dbSNP Id: rs994979916
• gnomAD v3: 7-151187366-T-C
• gnomAD v4: 7-151187366-T-C
• MyVariant Identifiers: chr7:g.150884453T>C (hg19) ; chr7:g.151187366T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187366T>C , CM000669.2:g.151187366T>C	GRCh38
NC_000007.13:g.150884453T>C , CM000669.1:g.150884453T>C	GRCh37
NC_000007.12:g.150515386T>C	NCBI36
NG_017016.1:g.5467A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275838.5:c.-236A>G	ENSP00000275838.1:n.-236A>G
ENST00000377867.7:c.271+86A>G	ENSP00000367098.3:n.271+86A>G
ENST00000415615.1:c.*9A>G	ENSP00000410871.1:n.*9A>G
NM_001142459.1:c.-236A>G	NP_001135931.2:n.-236A>G
NM_001142460.1:c.-236A>G	NP_001135932.2:n.-236A>G
NM_080871.3:c.271+86A>G	NP_543147.2:n.271+86A>G
NM_080871.4:c.271+86A>G	NP_543147.2:n.271+86A>G