Canonical Allele Identifier: CA10072433

Gene: COL6A2

Linked Data

• ClinVar Variation Id: 2147907
• ClinVar RCV Id: RCV003068582
• dbSNP Id: rs781603620
• ExAC: 21:47545799 T / C
• gnomAD v2: 21-47545799-T-C
• gnomAD v4: 21-46125885-T-C
• MyVariant Identifiers: chr21:g.47545799T>C (hg19) ; chr21:g.46125885T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46125885T>C , CM000683.2:g.46125885T>C	GRCh38
NC_000021.8:g.47545799T>C , CM000683.1:g.47545799T>C	GRCh37
NC_000021.7:g.46370227T>C	NCBI36
NG_008675.1:g.32767T>C , LRG_476:g.32767T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397763.6:c.2070T>C MANE Plus Clinical	ENSP00000380870.1:p.Ala690=
ENST00000300527.9:c.2070T>C MANE Select	ENSP00000300527.4:p.Ala690=
ENST00000409416.6:c.2070T>C	ENSP00000387115.1:p.Ala690=
ENST00000300527.8:c.2070T>C	ENSP00000300527.4:p.Ala690=
ENST00000310645.9:c.2070T>C	ENSP00000312529.5:p.Ala690=
ENST00000397763.5:c.2070T>C	ENSP00000380870.1:p.Ala690=
ENST00000409416.5:c.2070T>C	ENSP00000387115.1:p.Ala690=
ENST00000413758.1:c.741T>C	ENSP00000395751.1:p.Ala247=
NM_001849.3:c.2070T>C , LRG_476t1:c.2070T>C	NP_001840.3:p.Ala690=
NM_058174.2:c.2070T>C	NP_478054.2:p.Ala690=
NM_058175.2:c.2070T>C	NP_478055.2:p.Ala690=
XM_011529451.1:c.2070T>C	XP_011527753.1:p.Ala690=
XM_011529452.1:c.2070T>C	XP_011527754.1:p.Ala690=
XR_937438.1:n.2147T>C
XR_937439.1:n.2147T>C
XR_937438.2:n.2154T>C
XR_937439.2:n.2154T>C
NM_001849.4:c.2070T>C MANE Select	NP_001840.3:p.Ala690=
NM_058174.3:c.2070T>C MANE Plus Clinical	NP_478054.2:p.Ala690=
NM_058175.3:c.2070T>C	NP_478055.2:p.Ala690=