Canonical Allele Identifier: CA566410343

Gene: COL11A2

Linked Data

• dbSNP Id: rs1473370387
• gnomAD v2: 6-33160020-C-T
• gnomAD v3: 6-33192243-C-T
• gnomAD v4: 6-33192243-C-T
• MyVariant Identifiers: chr6:g.33160020C>T (hg19) ; chr6:g.33192243C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33192243C>T , CM000668.2:g.33192243C>T	GRCh38
NC_000006.11:g.33160020C>T , CM000668.1:g.33160020C>T	GRCh37
NC_000006.10:g.33267998C>T	NCBI36
NG_011589.1:g.5226G>A
NG_023374.1:g.13413G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000341947.7:c.-3G>A MANE Select	ENSP00000339915.2:n.-3G>A
ENST00000341947.6:c.-3G>A	ENSP00000339915.2:n.-3G>A
ENST00000361917.5:c.-3G>A	ENSP00000355123.1:n.-3G>A
ENST00000374708.8:c.-3G>A	ENSP00000363840.4:n.-3G>A
ENST00000395194.1:c.-3G>A	ENSP00000378620.1:n.-3G>A
ENST00000457788.5:c.-3G>A	ENSP00000405520.1:n.-3G>A
NM_001163771.1:c.-3G>A	NP_001157243.1:n.-3G>A
NM_080679.2:c.-3G>A	NP_542410.2:n.-3G>A
NM_080680.2:c.-3G>A	NP_542411.2:n.-3G>A
NM_080681.2:c.-3G>A	NP_542412.2:n.-3G>A
XM_011514298.1:c.-765+782G>A	XP_011512600.1:n.-765+782G>A
XM_017010250.1:c.-3G>A	XP_016865739.1:n.-3G>A
NM_001163771.2:c.-3G>A	NP_001157243.1:n.-3G>A
NM_080680.3:c.-3G>A MANE Select	NP_542411.2:n.-3G>A
NM_080681.3:c.-3G>A	NP_542412.2:n.-3G>A
NM_080679.3:c.-3G>A	NP_542410.2:n.-3G>A