Canonical Allele Identifier: CA321972000
Gene: COL6A1 HGNC NCBI

Linked Data

dbSNP Id: rs201757400
gnomAD v2: 21-47417522-G-A
gnomAD v3: 21-45997608-G-A
gnomAD v4: 21-45997608-G-A
MyVariant Identifiers: chr21:g.47417522G>A (hg19) chr21:g.45997608G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45997608G>A , CM000683.2:g.45997608G>A GRCh38
NC_000021.8:g.47417522G>A , CM000683.1:g.47417522G>A GRCh37
NC_000021.7:g.46241950G>A NCBI36
NG_008674.1:g.20860G>A , LRG_475:g.20860G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000683550.1:n.237-92G>A
ENST00000361866.8:c.1462-92G>A MANE Select ENSP00000355180.3:n.1462-92G>A
ENST00000361866.7:c.1462-92G>A ENSP00000355180.3:n.1462-92G>A
ENST00000612273.1:c.1462-92G>A ENSP00000483630.1:n.1462-92G>A
NM_001848.2:c.1462-92G>A , LRG_475t1:c.1462-92G>A NP_001839.2:n.1462-92G>A
NM_001848.3:c.1462-92G>A MANE Select NP_001839.2:n.1462-92G>A
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