Canonical Allele Identifier: CA10069940

Gene: COL6A1

Linked Data

• ClinVar Variation Id: 340311
• ClinVar RCV Id: RCV000337732 ; RCV000732805 ; RCV001501752
• dbSNP Id: rs200508160
• ExAC: 21:47410282 C / T
• gnomAD v2: 21-47410282-C-T
• gnomAD v3: 21-45990368-C-T
• gnomAD v4: 21-45990368-C-T
• MyVariant Identifiers: chr21:g.47410282C>T (hg19) ; chr21:g.45990368C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45990368C>T , CM000683.2:g.45990368C>T	GRCh38
NC_000021.8:g.47410282C>T , CM000683.1:g.47410282C>T	GRCh37
NC_000021.7:g.46234710C>T	NCBI36
NG_008674.1:g.13620C>T , LRG_475:g.13620C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361866.8:c.958-10C>T MANE Select	ENSP00000355180.3:n.958-10C>T
ENST00000361866.7:c.958-10C>T	ENSP00000355180.3:n.958-10C>T
ENST00000612273.1:c.958-10C>T	ENSP00000483630.1:n.958-10C>T
NM_001848.2:c.958-10C>T , LRG_475t1:c.958-10C>T	NP_001839.2:n.958-10C>T
NM_001848.3:c.958-10C>T MANE Select	NP_001839.2:n.958-10C>T