Canonical Allele Identifier: CA67839061

Gene: COL6A3

Linked Data

• dbSNP Id: rs75618738
• MyVariant Identifiers: chr2:g.238253070G>C (hg19) ; chr2:g.237344427G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344427G>C , CM000664.2:g.237344427G>C	GRCh38
NC_000002.11:g.238253070G>C , CM000664.1:g.238253070G>C	GRCh37
NC_000002.10:g.237917809G>C	NCBI36
NG_008676.1:g.74781C>G , LRG_473:g.74781C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.236C>G
ENST00000353578.9:c.6973C>G	ENSP00000315873.4:p.Leu2325Val
ENST00000295550.9:c.7591C>G MANE Select	ENSP00000295550.4:p.Leu2531Val
ENST00000295550.8:c.7591C>G	ENSP00000295550.4:p.Leu2531Val
ENST00000347401.7:c.5767C>G	ENSP00000315609.4:p.Leu1923Val
ENST00000353578.8:c.6973C>G	ENSP00000315873.4:p.Leu2325Val
ENST00000409809.5:c.6973C>G	ENSP00000386844.1:p.Leu2325Val
ENST00000472056.5:c.5770C>G	ENSP00000418285.1:p.Leu1924Val
ENST00000491769.1:n.1845C>G
NM_004369.3:c.7591C>G , LRG_473t1:c.7591C>G	NP_004360.2:p.Leu2531Val
NM_057166.4:c.5770C>G	NP_476507.3:p.Leu1924Val
NM_057167.3:c.6973C>G	NP_476508.2:p.Leu2325Val
XM_005246065.1:c.6991C>G	XP_005246122.1:p.Leu2331Val
XM_005246066.1:c.6370C>G	XP_005246123.1:p.Leu2124Val
XM_006712253.1:c.7090C>G	XP_006712316.1:p.Leu2364Val
XM_011510574.1:c.7588C>G	XP_011508876.1:p.Leu2530Val
XM_011510575.1:c.5185C>G	XP_011508877.1:p.Leu1729Val
XM_017003304.1:c.5185C>G	XP_016858793.1:p.Leu1729Val
XM_024452684.1:c.6370C>G	XP_024308452.1:p.Leu2124Val
NM_004369.4:c.7591C>G MANE Select	NP_004360.2:p.Leu2531Val
NM_057166.5:c.5770C>G	NP_476507.3:p.Leu1924Val
NM_057167.4:c.6973C>G	NP_476508.2:p.Leu2325Val