Canonical Allele Identifier: CA3751090
Gene: COL11A2 HGNC NCBI

Linked Data

dbSNP Id: rs121912945
gnomAD v2: 6-33144993-C-G
gnomAD v4: 6-33177216-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33177216C>G , CM000668.2:g.33177216C>G GRCh38
NC_000006.11:g.33144993C>G , CM000668.1:g.33144993C>G GRCh37
NC_000006.10:g.33252971C>G NCBI36
NG_011589.1:g.20253G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361917.6:c.554G>C
ENST00000341947.7:c.1981G>C MANE Select ENSP00000339915.2:p.Gly661Arg
ENST00000341947.6:c.1981G>C ENSP00000339915.2:p.Gly661Arg
ENST00000361917.5:c.1660G>C ENSP00000355123.1:p.Gly554Arg
ENST00000374708.8:c.1723G>C ENSP00000363840.4:p.Gly575Arg
ENST00000477772.1:n.200G>C
NM_080679.2:c.1660G>C NP_542410.2:p.Gly554Arg
NM_080680.2:c.1981G>C NP_542411.2:p.Gly661Arg
NM_080681.2:c.1723G>C NP_542412.2:p.Gly575Arg
XM_011514298.1:c.1135G>C XP_011512600.1:p.Gly379Arg
XM_011514299.1:c.1267G>C XP_011512601.1:p.Gly423Arg
XM_011514300.1:c.1087G>C XP_011512602.1:p.Gly363Arg
XM_011514301.1:c.1024G>C XP_011512603.1:p.Gly342Arg
XM_011514302.1:c.868G>C XP_011512604.1:p.Gly290Arg
XM_011514299.2:c.1267G>C XP_011512601.1:p.Gly423Arg
XM_011514300.2:c.1087G>C XP_011512602.1:p.Gly363Arg
XM_011514302.2:c.868G>C XP_011512604.1:p.Gly290Arg
XM_017010250.1:c.1981G>C XP_016865739.1:p.Gly661Arg
XM_017010251.2:c.799G>C XP_016865740.1:p.Gly267Arg
NM_080680.3:c.1981G>C MANE Select NP_542411.2:p.Gly661Arg
NM_080681.3:c.1723G>C NP_542412.2:p.Gly575Arg
NM_080679.3:c.1660G>C NP_542410.2:p.Gly554Arg