Canonical Allele Identifier: CA512717316
Gene: COL6A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.47417619C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45997705C>G , CM000683.2:g.45997705C>G GRCh38
NC_000021.8:g.47417619C>G , CM000683.1:g.47417619C>G GRCh37
NC_000021.7:g.46242047C>G NCBI36
NG_008674.1:g.20957C>G , LRG_475:g.20957C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000683550.1:n.242C>G
ENST00000361866.8:c.1467C>G MANE Select ENSP00000355180.3:p.Ala489=
ENST00000361866.7:c.1467C>G ENSP00000355180.3:p.Ala489=
ENST00000612273.1:c.1467C>G ENSP00000483630.1:p.Ala489=
NM_001848.2:c.1467C>G , LRG_475t1:c.1467C>G NP_001839.2:p.Ala489=
NM_001848.3:c.1467C>G MANE Select NP_001839.2:p.Ala489=
Search 100 bp 5'
Search 100 bp 3'