Canonical Allele Identifier: CA10071454
Gene: COL6A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283973
dbSNP Id: rs145500808

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46114058C>G , CM000683.2:g.46114058C>G GRCh38
NC_000021.8:g.47533972C>G , CM000683.1:g.47533972C>G GRCh37
NC_000021.7:g.46358400C>G NCBI36
NG_008675.1:g.20940C>G , LRG_476:g.20940C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000397763.6:c.786C>G MANE Plus Clinical ENSP00000380870.1:p.Gly262=
ENST00000300527.9:c.786C>G MANE Select ENSP00000300527.4:p.Gly262=
ENST00000409416.6:c.786C>G ENSP00000387115.1:p.Gly262=
ENST00000300527.8:c.786C>G ENSP00000300527.4:p.Gly262=
ENST00000310645.9:c.786C>G ENSP00000312529.5:p.Gly262=
ENST00000397763.5:c.786C>G ENSP00000380870.1:p.Gly262=
ENST00000409416.5:c.786C>G ENSP00000387115.1:p.Gly262=
ENST00000485591.1:n.442C>G
NM_001849.3:c.786C>G , LRG_476t1:c.786C>G NP_001840.3:p.Gly262=
NM_058174.2:c.786C>G NP_478054.2:p.Gly262=
NM_058175.2:c.786C>G NP_478055.2:p.Gly262=
XM_011529451.1:c.786C>G XP_011527753.1:p.Gly262=
XM_011529452.1:c.786C>G XP_011527754.1:p.Gly262=
XR_937438.1:n.909C>G
XR_937439.1:n.909C>G
XR_937438.2:n.916C>G
XR_937439.2:n.916C>G
NM_001849.4:c.786C>G MANE Select NP_001840.3:p.Gly262=
NM_058174.3:c.786C>G MANE Plus Clinical NP_478054.2:p.Gly262=
NM_058175.3:c.786C>G NP_478055.2:p.Gly262=