Canonical Allele Identifier: CA16609522

Gene: INA

Linked Data

• ClinVar Variation Id: 402160
• ClinVar RCV Id: RCV000454151
• dbSNP Id: rs920363358
• gnomAD v2: 10-105037530-G-A
• gnomAD v3: 10-103277773-G-A
• gnomAD v4: 10-103277773-G-A
• MyVariant Identifiers: chr10:g.105037530G>A (hg19) ; chr10:g.103277773G>A (hg38)
• PubMed: PMID:26539891

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103277773G>A , CM000672.2:g.103277773G>A	GRCh38
NC_000010.10:g.105037530G>A , CM000672.1:g.105037530G>A	GRCh37
NC_000010.9:g.105027520G>A	NCBI36
NG_012318.1:g.5611G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369849.9:c.562G>A MANE Select	ENSP00000358865.4:p.Gly188Arg
ENST00000369849.8:c.562G>A	ENSP00000358865.4:p.Gly188Arg
ENST00000616853.1:c.556G>A	ENSP00000481793.1:p.Gly186Arg
NM_032727.3:c.562G>A	NP_116116.1:p.Gly188Arg
NM_032727.4:c.562G>A MANE Select	NP_116116.1:p.Gly188Arg