Canonical Allele Identifier: CA431674904
Gene: COL6A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.238245118C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237336475C>T , CM000664.2:g.237336475C>T GRCh38
NC_000002.11:g.238245118C>T , CM000664.1:g.238245118C>T GRCh37
NC_000002.10:g.237909857C>T NCBI36
NG_008676.1:g.82733G>A , LRG_473:g.82733G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000347401.8:c.1270G>A
ENST00000353578.9:c.8007G>A ENSP00000315873.4:p.Lys2669=
ENST00000682957.1:c.752G>A
ENST00000684508.1:n.892G>A
ENST00000295550.9:c.8625G>A MANE Select ENSP00000295550.4:p.Lys2875=
ENST00000295550.8:c.8625G>A ENSP00000295550.4:p.Lys2875=
ENST00000347401.7:c.6801G>A ENSP00000315609.4:p.Lys2267=
ENST00000353578.8:c.8007G>A ENSP00000315873.4:p.Lys2669=
ENST00000409809.5:c.8007G>A ENSP00000386844.1:p.Lys2669=
ENST00000472056.5:c.6804G>A ENSP00000418285.1:p.Lys2268=
ENST00000491769.1:n.5067G>A
NM_004369.3:c.8625G>A , LRG_473t1:c.8625G>A NP_004360.2:p.Lys2875=
NM_057166.4:c.6804G>A NP_476507.3:p.Lys2268=
NM_057167.3:c.8007G>A NP_476508.2:p.Lys2669=
XM_005246065.1:c.8025G>A XP_005246122.1:p.Lys2675=
XM_005246066.1:c.7404G>A XP_005246123.1:p.Lys2468=
XM_006712253.1:c.8124G>A XP_006712316.1:p.Lys2708=
XM_011510574.1:c.8622G>A XP_011508876.1:p.Lys2874=
XM_011510575.1:c.6219G>A XP_011508877.1:p.Lys2073=
XM_017003304.1:c.6219G>A XP_016858793.1:p.Lys2073=
XM_024452684.1:c.7404G>A XP_024308452.1:p.Lys2468=
NM_004369.4:c.8625G>A MANE Select NP_004360.2:p.Lys2875=
NM_057166.5:c.6804G>A NP_476507.3:p.Lys2268=
NM_057167.4:c.8007G>A NP_476508.2:p.Lys2669=