Canonical Allele Identifier: CA579077295

Gene: ASB10

Linked Data

• dbSNP Id: rs1184961900
• gnomAD v2: 7-150884406-G-C
• gnomAD v4: 7-151187319-G-C
• MyVariant Identifiers: chr7:g.150884406G>C (hg19) ; chr7:g.151187319G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187319G>C , CM000669.2:g.151187319G>C	GRCh38
NC_000007.13:g.150884406G>C , CM000669.1:g.150884406G>C	GRCh37
NC_000007.12:g.150515339G>C	NCBI36
NG_017016.1:g.5514C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275838.5:c.-189C>G	ENSP00000275838.1:n.-189C>G
ENST00000377867.7:c.271+133C>G	ENSP00000367098.3:n.271+133C>G
ENST00000415615.1:c.*56C>G	ENSP00000410871.1:n.*56C>G
NM_001142459.1:c.-189C>G	NP_001135931.2:n.-189C>G
NM_001142460.1:c.-189C>G	NP_001135932.2:n.-189C>G
NM_080871.3:c.271+133C>G	NP_543147.2:n.271+133C>G
NM_080871.4:c.271+133C>G	NP_543147.2:n.271+133C>G