Canonical Allele Identifier: CA137061560

Gene: COL11A2

Linked Data

• dbSNP Id: rs760954641
• gnomAD v3: 6-33164615-G-A
• gnomAD v4: 6-33164615-G-A
• MyVariant Identifiers: chr6:g.33132392G>A (hg19) ; chr6:g.33164615G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164615G>A , CM000668.2:g.33164615G>A	GRCh38
NC_000006.11:g.33132392G>A , CM000668.1:g.33132392G>A	GRCh37
NC_000006.10:g.33240370G>A	NCBI36
NG_011589.1:g.32854C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.670-142C>T
ENST00000341947.7:c.4864-142C>T MANE Select	ENSP00000339915.2:n.4864-142C>T
ENST00000341947.6:c.4864-142C>T	ENSP00000339915.2:n.4864-142C>T
ENST00000361917.5:c.4543-142C>T	ENSP00000355123.1:n.4543-142C>T
ENST00000374708.8:c.4606-142C>T	ENSP00000363840.4:n.4606-142C>T
ENST00000477772.1:n.654-142C>T
NM_080679.2:c.4543-142C>T	NP_542410.2:n.4543-142C>T
NM_080680.2:c.4864-142C>T	NP_542411.2:n.4864-142C>T
NM_080681.2:c.4606-142C>T	NP_542412.2:n.4606-142C>T
XM_011514298.1:c.4018-142C>T	XP_011512600.1:n.4018-142C>T
XM_011514299.1:c.4150-142C>T	XP_011512601.1:n.4150-142C>T
XM_011514300.1:c.3970-142C>T	XP_011512602.1:n.3970-142C>T
XM_011514301.1:c.3907-142C>T	XP_011512603.1:n.3907-142C>T
XM_011514302.1:c.3751-142C>T	XP_011512604.1:n.3751-142C>T
XM_011514299.2:c.4150-142C>T	XP_011512601.1:n.4150-142C>T
XM_011514300.2:c.3970-142C>T	XP_011512602.1:n.3970-142C>T
XM_011514302.2:c.3751-142C>T	XP_011512604.1:n.3751-142C>T
XM_017010250.1:c.4864-142C>T	XP_016865739.1:n.4864-142C>T
XM_017010251.2:c.3682-142C>T	XP_016865740.1:n.3682-142C>T
NM_080680.3:c.4864-142C>T MANE Select	NP_542411.2:n.4864-142C>T
NM_080681.3:c.4606-142C>T	NP_542412.2:n.4606-142C>T
NM_080679.3:c.4543-142C>T	NP_542410.2:n.4543-142C>T