Canonical Allele Identifier: CA512728357

Gene: COL6A2

Linked Data

• MyVariant Identifiers: chr21:g.47541481A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46121567A>T , CM000683.2:g.46121567A>T	GRCh38
NC_000021.8:g.47541481A>T , CM000683.1:g.47541481A>T	GRCh37
NC_000021.7:g.46365909A>T	NCBI36
NG_008675.1:g.28449A>T , LRG_476:g.28449A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000397763.6:c.1470A>T MANE Plus Clinical	ENSP00000380870.1:p.Gly490=
ENST00000300527.9:c.1470A>T MANE Select	ENSP00000300527.4:p.Gly490=
ENST00000409416.6:c.1470A>T	ENSP00000387115.1:p.Gly490=
ENST00000300527.8:c.1470A>T	ENSP00000300527.4:p.Gly490=
ENST00000310645.9:c.1470A>T	ENSP00000312529.5:p.Gly490=
ENST00000397763.5:c.1470A>T	ENSP00000380870.1:p.Gly490=
ENST00000409416.5:c.1470A>T	ENSP00000387115.1:p.Gly490=
ENST00000413758.1:c.93A>T	ENSP00000395751.1:p.Gly31=
NM_001849.3:c.1470A>T , LRG_476t1:c.1470A>T	NP_001840.3:p.Gly490=
NM_058174.2:c.1470A>T	NP_478054.2:p.Gly490=
NM_058175.2:c.1470A>T	NP_478055.2:p.Gly490=
XM_011529451.1:c.1470A>T	XP_011527753.1:p.Gly490=
XM_011529452.1:c.1470A>T	XP_011527754.1:p.Gly490=
XR_937438.1:n.1593A>T
XR_937439.1:n.1593A>T
XR_937438.2:n.1600A>T
XR_937439.2:n.1600A>T
NM_001849.4:c.1470A>T MANE Select	NP_001840.3:p.Gly490=
NM_058174.3:c.1470A>T MANE Plus Clinical	NP_478054.2:p.Gly490=
NM_058175.3:c.1470A>T	NP_478055.2:p.Gly490=