Canonical Allele Identifier: CA10069514
Gene: COL6A1 HGNC NCBI

Linked Data

dbSNP Id: rs776938323

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45984311G>A , CM000683.2:g.45984311G>A GRCh38
NC_000021.8:g.47404225G>A , CM000683.1:g.47404225G>A GRCh37
NC_000021.7:g.46228653G>A NCBI36
NG_008674.1:g.7563G>A , LRG_475:g.7563G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361866.8:c.270G>A MANE Select ENSP00000355180.3:p.Ala90=
ENST00000361866.7:c.270G>A ENSP00000355180.3:p.Ala90=
ENST00000612273.1:c.270G>A ENSP00000483630.1:p.Ala90=
NM_001848.2:c.270G>A , LRG_475t1:c.270G>A NP_001839.2:p.Ala90=
NM_001848.3:c.270G>A MANE Select NP_001839.2:p.Ala90=