Canonical Allele Identifier: CA10069561

Gene: COL6A1

Linked Data

• ClinVar Variation Id: 258301
• ClinVar RCV Id: RCV000250435 ; RCV000525643 ; RCV000726612
• dbSNP Id: rs373486149
• ExAC: 21:47404378 C / T
• gnomAD v2: 21-47404378-C-T
• gnomAD v3: 21-45984464-C-T
• gnomAD v4: 21-45984464-C-T
• MyVariant Identifiers: chr21:g.47404378C>T (hg19) ; chr21:g.45984464C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45984464C>T , CM000683.2:g.45984464C>T	GRCh38
NC_000021.8:g.47404378C>T , CM000683.1:g.47404378C>T	GRCh37
NC_000021.7:g.46228806C>T	NCBI36
NG_008674.1:g.7716C>T , LRG_475:g.7716C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361866.8:c.423C>T MANE Select	ENSP00000355180.3:p.Leu141=
ENST00000361866.7:c.423C>T	ENSP00000355180.3:p.Leu141=
ENST00000612273.1:c.423C>T	ENSP00000483630.1:p.Leu141=
NM_001848.2:c.423C>T , LRG_475t1:c.423C>T	NP_001839.2:p.Leu141=
NM_001848.3:c.423C>T MANE Select	NP_001839.2:p.Leu141=