Canonical Allele Identifier: CA1619890238
Gene: COL11A2 HGNC NCBI

Linked Data

dbSNP Id: rs1023583380
gnomAD v4: 6-33164751-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33164751G>T , CM000668.2:g.33164751G>T GRCh38
NC_000006.11:g.33132528G>T , CM000668.1:g.33132528G>T GRCh37
NC_000006.10:g.33240506G>T NCBI36
NG_011589.1:g.32718C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000683572.1:n.669+101C>A
ENST00000341947.7:c.4863+101C>A MANE Select ENSP00000339915.2:n.4863+101C>A
ENST00000341947.6:c.4863+101C>A ENSP00000339915.2:n.4863+101C>A
ENST00000361917.5:c.4542+101C>A ENSP00000355123.1:n.4542+101C>A
ENST00000374708.8:c.4605+101C>A ENSP00000363840.4:n.4605+101C>A
ENST00000477772.1:n.653+101C>A
NM_080679.2:c.4542+101C>A NP_542410.2:n.4542+101C>A
NM_080680.2:c.4863+101C>A NP_542411.2:n.4863+101C>A
NM_080681.2:c.4605+101C>A NP_542412.2:n.4605+101C>A
XM_011514298.1:c.4017+101C>A XP_011512600.1:n.4017+101C>A
XM_011514299.1:c.4149+101C>A XP_011512601.1:n.4149+101C>A
XM_011514300.1:c.3969+101C>A XP_011512602.1:n.3969+101C>A
XM_011514301.1:c.3906+101C>A XP_011512603.1:n.3906+101C>A
XM_011514302.1:c.3750+101C>A XP_011512604.1:n.3750+101C>A
XM_011514299.2:c.4149+101C>A XP_011512601.1:n.4149+101C>A
XM_011514300.2:c.3969+101C>A XP_011512602.1:n.3969+101C>A
XM_011514302.2:c.3750+101C>A XP_011512604.1:n.3750+101C>A
XM_017010250.1:c.4863+101C>A XP_016865739.1:n.4863+101C>A
XM_017010251.2:c.3681+101C>A XP_016865740.1:n.3681+101C>A
NM_080680.3:c.4863+101C>A MANE Select NP_542411.2:n.4863+101C>A
NM_080681.3:c.4605+101C>A NP_542412.2:n.4605+101C>A
NM_080679.3:c.4542+101C>A NP_542410.2:n.4542+101C>A