Canonical Allele Identifier: CA10069565
Gene: COL6A1 HGNC NCBI

Linked Data

dbSNP Id: rs757243602

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45984473A>G , CM000683.2:g.45984473A>G GRCh38
NC_000021.8:g.47404387A>G , CM000683.1:g.47404387A>G GRCh37
NC_000021.7:g.46228815A>G NCBI36
NG_008674.1:g.7725A>G , LRG_475:g.7725A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361866.8:c.428+4A>G MANE Select ENSP00000355180.3:n.428+4A>G
ENST00000361866.7:c.428+4A>G ENSP00000355180.3:n.428+4A>G
ENST00000612273.1:c.428+4A>G ENSP00000483630.1:n.428+4A>G
NM_001848.2:c.428+4A>G , LRG_475t1:c.428+4A>G NP_001839.2:n.428+4A>G
NM_001848.3:c.428+4A>G MANE Select NP_001839.2:n.428+4A>G