Canonical Allele Identifier: CA449867296

Gene: COL11A2

Linked Data

• dbSNP Id: rs1244875580
• gnomAD v2: 6-33132680-G-A
• gnomAD v4: 6-33164903-G-A
• MyVariant Identifiers: chr6:g.33132680G>A (hg19) ; chr6:g.33164903G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164903G>A , CM000668.2:g.33164903G>A	GRCh38
NC_000006.11:g.33132680G>A , CM000668.1:g.33132680G>A	GRCh37
NC_000006.10:g.33240658G>A	NCBI36
NG_011589.1:g.32566C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.618C>T
ENST00000341947.7:c.4812C>T MANE Select	ENSP00000339915.2:p.Asn1604=
ENST00000341947.6:c.4812C>T	ENSP00000339915.2:p.Asn1604=
ENST00000361917.5:c.4491C>T	ENSP00000355123.1:p.Asn1497=
ENST00000374708.8:c.4554C>T	ENSP00000363840.4:p.Asn1518=
ENST00000477772.1:n.602C>T
NM_080679.2:c.4491C>T	NP_542410.2:p.Asn1497=
NM_080680.2:c.4812C>T	NP_542411.2:p.Asn1604=
NM_080681.2:c.4554C>T	NP_542412.2:p.Asn1518=
XM_011514298.1:c.3966C>T	XP_011512600.1:p.Asn1322=
XM_011514299.1:c.4098C>T	XP_011512601.1:p.Asn1366=
XM_011514300.1:c.3918C>T	XP_011512602.1:p.Asn1306=
XM_011514301.1:c.3855C>T	XP_011512603.1:p.Asn1285=
XM_011514302.1:c.3699C>T	XP_011512604.1:p.Asn1233=
XM_011514299.2:c.4098C>T	XP_011512601.1:p.Asn1366=
XM_011514300.2:c.3918C>T	XP_011512602.1:p.Asn1306=
XM_011514302.2:c.3699C>T	XP_011512604.1:p.Asn1233=
XM_017010250.1:c.4812C>T	XP_016865739.1:p.Asn1604=
XM_017010251.2:c.3630C>T	XP_016865740.1:p.Asn1210=
NM_080680.3:c.4812C>T MANE Select	NP_542411.2:p.Asn1604=
NM_080681.3:c.4554C>T	NP_542412.2:p.Asn1518=
NM_080679.3:c.4491C>T	NP_542410.2:p.Asn1497=