Canonical Allele Identifier: CA10071002

Gene: COL6A1

Linked Data

• ClinVar Variation Id: 497505
• ClinVar RCV Id: RCV000597984 ; RCV001088514
• dbSNP Id: rs372931456
• ExAC: 21:47423534 G / A
• gnomAD v2: 21-47423534-G-A
• gnomAD v3: 21-46003620-G-A
• gnomAD v4: 21-46003620-G-A
• MyVariant Identifiers: chr21:g.47423534G>A (hg19) ; chr21:g.46003620G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46003620G>A , CM000683.2:g.46003620G>A	GRCh38
NC_000021.8:g.47423534G>A , CM000683.1:g.47423534G>A	GRCh37
NC_000021.7:g.46247962G>A	NCBI36
NG_008674.1:g.26872G>A , LRG_475:g.26872G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463060.6:n.1093G>A
ENST00000612273.2:c.820G>A
ENST00000682634.1:c.820G>A
ENST00000361866.8:c.2694G>A MANE Select	ENSP00000355180.3:p.Thr898=
ENST00000361866.7:c.2694G>A	ENSP00000355180.3:p.Thr898=
ENST00000486023.1:n.482G>A
ENST00000498614.5:n.928G>A
ENST00000612273.1:c.2688G>A	ENSP00000483630.1:p.Thr896=
NM_001848.2:c.2694G>A , LRG_475t1:c.2694G>A	NP_001839.2:p.Thr898=
NM_001848.3:c.2694G>A MANE Select	NP_001839.2:p.Thr898=