Canonical Allele Identifier: CA579077298

Gene: ASB10

Linked Data

• dbSNP Id: rs760704096
• gnomAD v2: 7-150884429-C-G
• gnomAD v3: 7-151187342-C-G
• gnomAD v4: 7-151187342-C-G
• MyVariant Identifiers: chr7:g.150884429C>G (hg19) ; chr7:g.151187342C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187342C>G , CM000669.2:g.151187342C>G	GRCh38
NC_000007.13:g.150884429C>G , CM000669.1:g.150884429C>G	GRCh37
NC_000007.12:g.150515362C>G	NCBI36
NG_017016.1:g.5491G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275838.5:c.-212G>C	ENSP00000275838.1:n.-212G>C
ENST00000377867.7:c.271+110G>C	ENSP00000367098.3:n.271+110G>C
ENST00000415615.1:c.*33G>C	ENSP00000410871.1:n.*33G>C
NM_001142459.1:c.-212G>C	NP_001135931.2:n.-212G>C
NM_001142460.1:c.-212G>C	NP_001135932.2:n.-212G>C
NM_080871.3:c.271+110G>C	NP_543147.2:n.271+110G>C
NM_080871.4:c.271+110G>C	NP_543147.2:n.271+110G>C