Canonical Allele Identifier: CA10070532

Gene: COL6A1

Linked Data

• ClinVar Variation Id: 502579
• ClinVar RCV Id: RCV000592845 ; RCV001089428 ; RCV003126841
• dbSNP Id: rs200334019
• ExAC: 21:47419565 G / A
• gnomAD v2: 21-47419565-G-A
• gnomAD v3: 21-45999651-G-A
• gnomAD v4: 21-45999651-G-A
• MyVariant Identifiers: chr21:g.47419565G>A (hg19) ; chr21:g.45999651G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45999651G>A , CM000683.2:g.45999651G>A	GRCh38
NC_000021.8:g.47419565G>A , CM000683.1:g.47419565G>A	GRCh37
NC_000021.7:g.46243993G>A	NCBI36
NG_008674.1:g.22903G>A , LRG_475:g.22903G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361866.8:c.1741-6G>A MANE Select	ENSP00000355180.3:n.1741-6G>A
ENST00000361866.7:c.1741-6G>A	ENSP00000355180.3:n.1741-6G>A
ENST00000466285.1:n.252G>A
ENST00000612273.1:c.1741-6G>A	ENSP00000483630.1:n.1741-6G>A
NM_001848.2:c.1741-6G>A , LRG_475t1:c.1741-6G>A	NP_001839.2:n.1741-6G>A
NM_001848.3:c.1741-6G>A MANE Select	NP_001839.2:n.1741-6G>A