Canonical Allele Identifier: CA4573966

Gene: ASB10

Linked Data

• dbSNP Id: rs780378243
• ExAC: 7:150884008 G / T
• gnomAD v2: 7-150884008-G-T
• MyVariant Identifiers: chr7:g.150884008G>T (hg19) ; chr7:g.151186921G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186921G>T , CM000669.2:g.151186921G>T	GRCh38
NC_000007.13:g.150884008G>T , CM000669.1:g.150884008G>T	GRCh37
NC_000007.12:g.150514941G>T	NCBI36
NG_017016.1:g.5912C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000420175.3:c.210C>A MANE Select	ENSP00000391137.2:p.Val70=
ENST00000275838.5:c.210C>A	ENSP00000275838.1:p.Val70=
ENST00000377867.7:c.272-262C>A	ENSP00000367098.3:n.272-262C>A
ENST00000415615.1:c.*254C>A	ENSP00000410871.1:n.*254C>A
ENST00000420175.2:c.210C>A	ENSP00000391137.2:p.Val70=
NM_001142459.1:c.210C>A	NP_001135931.2:p.Val70=
NM_001142460.1:c.210C>A	NP_001135932.2:p.Val70=
NM_080871.3:c.272-262C>A	NP_543147.2:n.272-262C>A
XM_005249949.3:c.345C>A	XP_005250006.1:p.Val115=
NM_001142459.2:c.210C>A MANE Select	NP_001135931.2:p.Val70=
NM_080871.4:c.272-262C>A	NP_543147.2:n.272-262C>A