Canonical Allele Identifier: CA658799471
Gene: COL6A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 497048
ClinVar RCV Id: RCV000591139
dbSNP Id: rs1555872143

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46114001_46114011del , CM000683.2:g.46114001_46114011del GRCh38
NC_000021.8:g.47533915_47533925del , CM000683.1:g.47533915_47533925del GRCh37
NC_000021.7:g.46358343_46358353del NCBI36
NG_008675.1:g.20883_20893del , LRG_476:g.20883_20893del

Transcript Alleles

HGVS Amino-acid change
ENST00000397763.6:c.736-7_739del
ENST00000300527.9:c.736-7_739del
ENST00000409416.6:c.736-7_739del
ENST00000300527.8:c.736-7_739del
ENST00000310645.9:c.736-7_739del
ENST00000397763.5:c.736-7_739del
ENST00000409416.5:c.736-7_739del
ENST00000485591.1:n.385_395del
NM_001849.3:c.736-7_739del , LRG_476t1:c.736-7_739del
NM_058174.2:c.736-7_739del
NM_058175.2:c.736-7_739del
XM_011529451.1:c.736-7_739del
XM_011529452.1:c.736-7_739del
XR_937438.1:n.859-7_862del
XR_937439.1:n.859-7_862del
XR_937438.2:n.866-7_869del
XR_937439.2:n.866-7_869del
NM_001849.4:c.736-7_739del
NM_058174.3:c.736-7_739del
NM_058175.3:c.736-7_739del