Canonical Allele Identifier: CA512718645
Gene: COL6A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.47421276G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46001362G>T , CM000683.2:g.46001362G>T GRCh38
NC_000021.8:g.47421276G>T , CM000683.1:g.47421276G>T GRCh37
NC_000021.7:g.46245704G>T NCBI36
NG_008674.1:g.24614G>T , LRG_475:g.24614G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463060.6:n.331G>T
ENST00000612273.2:c.58G>T
ENST00000682634.1:c.58G>T
ENST00000361866.8:c.1932G>T MANE Select ENSP00000355180.3:p.Arg644=
ENST00000361866.7:c.1932G>T ENSP00000355180.3:p.Arg644=
ENST00000463060.5:n.331G>T
ENST00000498614.5:n.166G>T
ENST00000612273.1:c.1926G>T ENSP00000483630.1:p.Arg642=
NM_001848.2:c.1932G>T , LRG_475t1:c.1932G>T NP_001839.2:p.Arg644=
NM_001848.3:c.1932G>T MANE Select NP_001839.2:p.Arg644=