Canonical Allele Identifier: CA749801466

Gene: COL6A2

Linked Data

• dbSNP Id: rs1362731623
• MyVariant Identifiers: chr21:g.47535744C>G (hg19) ; chr21:g.46115830C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46115830C>G , CM000683.2:g.46115830C>G	GRCh38
NC_000021.8:g.47535744C>G , CM000683.1:g.47535744C>G	GRCh37
NC_000021.7:g.46360172C>G	NCBI36
NG_008675.1:g.22712C>G , LRG_476:g.22712C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397763.6:c.802-42C>G MANE Plus Clinical	ENSP00000380870.1:n.802-42C>G
ENST00000300527.9:c.802-42C>G MANE Select	ENSP00000300527.4:n.802-42C>G
ENST00000409416.6:c.802-42C>G	ENSP00000387115.1:n.802-42C>G
ENST00000300527.8:c.802-42C>G	ENSP00000300527.4:n.802-42C>G
ENST00000310645.9:c.802-42C>G	ENSP00000312529.5:n.802-42C>G
ENST00000397763.5:c.802-42C>G	ENSP00000380870.1:n.802-42C>G
ENST00000409416.5:c.802-42C>G	ENSP00000387115.1:n.802-42C>G
ENST00000485591.1:n.458-42C>G
NM_001849.3:c.802-42C>G , LRG_476t1:c.802-42C>G	NP_001840.3:n.802-42C>G
NM_058174.2:c.802-42C>G	NP_478054.2:n.802-42C>G
NM_058175.2:c.802-42C>G	NP_478055.2:n.802-42C>G
XM_011529451.1:c.802-42C>G	XP_011527753.1:n.802-42C>G
XM_011529452.1:c.802-42C>G	XP_011527754.1:n.802-42C>G
XR_937438.1:n.925-42C>G
XR_937439.1:n.925-42C>G
XR_937438.2:n.932-42C>G
XR_937439.2:n.932-42C>G
NM_001849.4:c.802-42C>G MANE Select	NP_001840.3:n.802-42C>G
NM_058174.3:c.802-42C>G MANE Plus Clinical	NP_478054.2:n.802-42C>G
NM_058175.3:c.802-42C>G	NP_478055.2:n.802-42C>G