Canonical Allele Identifier: CA137061836

Gene: COL11A2

Linked Data

• dbSNP Id: rs894477408
• gnomAD v2: 6-33132894-A-G
• gnomAD v3: 6-33165117-A-G
• gnomAD v4: 6-33165117-A-G
• MyVariant Identifiers: chr6:g.33132894A>G (hg19) ; chr6:g.33165117A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33165117A>G , CM000668.2:g.33165117A>G	GRCh38
NC_000006.11:g.33132894A>G , CM000668.1:g.33132894A>G	GRCh37
NC_000006.10:g.33240872A>G	NCBI36
NG_011589.1:g.32352T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.557-153T>C
ENST00000341947.7:c.4751-153T>C MANE Select	ENSP00000339915.2:n.4751-153T>C
ENST00000341947.6:c.4751-153T>C	ENSP00000339915.2:n.4751-153T>C
ENST00000361917.5:c.4430-153T>C	ENSP00000355123.1:n.4430-153T>C
ENST00000374708.8:c.4493-153T>C	ENSP00000363840.4:n.4493-153T>C
ENST00000477772.1:n.541-153T>C
NM_080679.2:c.4430-153T>C	NP_542410.2:n.4430-153T>C
NM_080680.2:c.4751-153T>C	NP_542411.2:n.4751-153T>C
NM_080681.2:c.4493-153T>C	NP_542412.2:n.4493-153T>C
XM_011514298.1:c.3905-153T>C	XP_011512600.1:n.3905-153T>C
XM_011514299.1:c.4037-153T>C	XP_011512601.1:n.4037-153T>C
XM_011514300.1:c.3857-153T>C	XP_011512602.1:n.3857-153T>C
XM_011514301.1:c.3794-153T>C	XP_011512603.1:n.3794-153T>C
XM_011514302.1:c.3638-153T>C	XP_011512604.1:n.3638-153T>C
XM_011514299.2:c.4037-153T>C	XP_011512601.1:n.4037-153T>C
XM_011514300.2:c.3857-153T>C	XP_011512602.1:n.3857-153T>C
XM_011514302.2:c.3638-153T>C	XP_011512604.1:n.3638-153T>C
XM_017010250.1:c.4751-153T>C	XP_016865739.1:n.4751-153T>C
XM_017010251.2:c.3569-153T>C	XP_016865740.1:n.3569-153T>C
NM_080680.3:c.4751-153T>C MANE Select	NP_542411.2:n.4751-153T>C
NM_080681.3:c.4493-153T>C	NP_542412.2:n.4493-153T>C
NM_080679.3:c.4430-153T>C	NP_542410.2:n.4430-153T>C