Canonical Allele Identifier: CA370035957

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186482-T-C
• MyVariant Identifiers: chr7:g.150883569T>C (hg19) ; chr7:g.151186482T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186482T>C , CM000669.2:g.151186482T>C	GRCh38
NC_000007.13:g.150883569T>C , CM000669.1:g.150883569T>C	GRCh37
NC_000007.12:g.150514502T>C	NCBI36
NG_017016.1:g.6351A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.494A>G MANE Select	ENSP00000391137.2:p.His165Arg
ENST00000275838.5:c.494A>G	ENSP00000275838.1:p.His165Arg
ENST00000377867.7:c.449A>G	ENSP00000367098.3:p.His150Arg
ENST00000420175.2:c.494A>G	ENSP00000391137.2:p.His165Arg
NM_001142459.1:c.494A>G	NP_001135931.2:p.His165Arg
NM_001142460.1:c.494A>G	NP_001135932.2:p.His165Arg
NM_080871.3:c.449A>G	NP_543147.2:p.His150Arg
XM_005249949.3:c.629A>G	XP_005250006.1:p.His210Arg
NM_001142459.2:c.494A>G MANE Select	NP_001135931.2:p.His165Arg
NM_080871.4:c.449A>G	NP_543147.2:p.His150Arg