Canonical Allele Identifier: CA566410340

Gene: COL11A2

Linked Data

• dbSNP Id: rs1237273497
• gnomAD v2: 6-33160018-G-A
• gnomAD v3: 6-33192241-G-A
• gnomAD v4: 6-33192241-G-A
• MyVariant Identifiers: chr6:g.33160018G>A (hg19) ; chr6:g.33192241G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33192241G>A , CM000668.2:g.33192241G>A	GRCh38
NC_000006.11:g.33160018G>A , CM000668.1:g.33160018G>A	GRCh37
NC_000006.10:g.33267996G>A	NCBI36
NG_011589.1:g.5228C>T
NG_023374.1:g.13415C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000341947.7:c.-1C>T MANE Select	ENSP00000339915.2:n.-1C>T
ENST00000341947.6:c.-1C>T	ENSP00000339915.2:n.-1C>T
ENST00000361917.5:c.-1C>T	ENSP00000355123.1:n.-1C>T
ENST00000374708.8:c.-1C>T	ENSP00000363840.4:n.-1C>T
ENST00000395194.1:c.-1C>T	ENSP00000378620.1:n.-1C>T
ENST00000457788.5:c.-1C>T	ENSP00000405520.1:n.-1C>T
NM_001163771.1:c.-1C>T	NP_001157243.1:n.-1C>T
NM_080679.2:c.-1C>T	NP_542410.2:n.-1C>T
NM_080680.2:c.-1C>T	NP_542411.2:n.-1C>T
NM_080681.2:c.-1C>T	NP_542412.2:n.-1C>T
XM_011514298.1:c.-765+784C>T	XP_011512600.1:n.-765+784C>T
XM_017010250.1:c.-1C>T	XP_016865739.1:n.-1C>T
NM_001163771.2:c.-1C>T	NP_001157243.1:n.-1C>T
NM_080680.3:c.-1C>T MANE Select	NP_542411.2:n.-1C>T
NM_080681.3:c.-1C>T	NP_542412.2:n.-1C>T
NM_080679.3:c.-1C>T	NP_542410.2:n.-1C>T