Canonical Allele Identifier: CA513169064
Gene: COL6A1 HGNC NCBI

Linked Data

dbSNP Id: rs1364102125
MyVariant Identifiers: chr21:g.47404267G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45984353G>T , CM000683.2:g.45984353G>T GRCh38
NC_000021.8:g.47404267G>T , CM000683.1:g.47404267G>T GRCh37
NC_000021.7:g.46228695G>T NCBI36
NG_008674.1:g.7605G>T , LRG_475:g.7605G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361866.8:c.312G>T MANE Select ENSP00000355180.3:p.Thr104=
ENST00000361866.7:c.312G>T ENSP00000355180.3:p.Thr104=
ENST00000612273.1:c.312G>T ENSP00000483630.1:p.Thr104=
NM_001848.2:c.312G>T , LRG_475t1:c.312G>T NP_001839.2:p.Thr104=
NM_001848.3:c.312G>T MANE Select NP_001839.2:p.Thr104=