Canonical Allele Identifier: CA2189319
Gene: COL6A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 500557
dbSNP Id: rs116256579

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237377034G>A , CM000664.2:g.237377034G>A GRCh38
NC_000002.11:g.238285677G>A , CM000664.1:g.238285677G>A GRCh37
NC_000002.10:g.237950416G>A NCBI36
NG_008676.1:g.42174C>T , LRG_473:g.42174C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000353578.9:c.2190C>T ENSP00000315873.4:p.Ile730=
ENST00000295550.9:c.2808C>T MANE Select ENSP00000295550.4:p.Ile936=
ENST00000295550.8:c.2808C>T ENSP00000295550.4:p.Ile936=
ENST00000347401.7:c.987C>T ENSP00000315609.4:p.Ile329=
ENST00000353578.8:c.2190C>T ENSP00000315873.4:p.Ile730=
ENST00000392003.6:c.1587C>T ENSP00000375860.2:p.Ile529=
ENST00000392004.7:c.2190C>T ENSP00000375861.3:p.Ile730=
ENST00000409809.5:c.2190C>T ENSP00000386844.1:p.Ile730=
ENST00000472056.5:c.987C>T ENSP00000418285.1:p.Ile329=
NM_004369.3:c.2808C>T , LRG_473t1:c.2808C>T NP_004360.2:p.Ile936=
NM_057164.4:c.1587C>T NP_476505.3:p.Ile529=
NM_057165.4:c.2190C>T NP_476506.3:p.Ile730=
NM_057166.4:c.987C>T NP_476507.3:p.Ile329=
NM_057167.3:c.2190C>T NP_476508.2:p.Ile730=
XM_005246065.1:c.2208C>T XP_005246122.1:p.Ile736=
XM_005246066.1:c.1587C>T XP_005246123.1:p.Ile529=
XM_006712253.1:c.2808C>T XP_006712316.1:p.Ile936=
XM_011510574.1:c.2808C>T XP_011508876.1:p.Ile936=
XM_011510575.1:c.402C>T XP_011508877.1:p.Ile134=
XM_017003304.1:c.402C>T XP_016858793.1:p.Ile134=
XM_024452684.1:c.1587C>T XP_024308452.1:p.Ile529=
NM_004369.4:c.2808C>T MANE Select NP_004360.2:p.Ile936=
NM_057164.5:c.1587C>T NP_476505.3:p.Ile529=
NM_057165.5:c.2190C>T NP_476506.3:p.Ile730=
NM_057166.5:c.987C>T NP_476507.3:p.Ile329=
NM_057167.4:c.2190C>T NP_476508.2:p.Ile730=