Canonical Allele Identifier: CA512717317
Gene: COL6A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.47417620A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45997706A>C , CM000683.2:g.45997706A>C GRCh38
NC_000021.8:g.47417620A>C , CM000683.1:g.47417620A>C GRCh37
NC_000021.7:g.46242048A>C NCBI36
NG_008674.1:g.20958A>C , LRG_475:g.20958A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000683550.1:n.243A>C
ENST00000361866.8:c.1468A>C MANE Select ENSP00000355180.3:p.Arg490=
ENST00000361866.7:c.1468A>C ENSP00000355180.3:p.Arg490=
ENST00000612273.1:c.1468A>C ENSP00000483630.1:p.Arg490=
NM_001848.2:c.1468A>C , LRG_475t1:c.1468A>C NP_001839.2:p.Arg490=
NM_001848.3:c.1468A>C MANE Select NP_001839.2:p.Arg490=