Canonical Allele Identifier: CA2669560520

Gene: FGFR3

Linked Data

• gnomAD v4: 4-1801365-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1801369del , CM000666.2:g.1801369del	GRCh38
NC_000004.11:g.1803096del , CM000666.1:g.1803096del	GRCh37
NC_000004.10:g.1772894del	NCBI36
NG_012632.1:g.13058del , LRG_1021:g.13058del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340107.9:c.448del
ENST00000260795.8:c.448del
ENST00000352904.6:c.448del
ENST00000412135.7:c.436del
ENST00000440486.8:c.448del
ENST00000481110.7:c.448del
ENST00000260795.6:c.448del
ENST00000340107.8:c.448del
ENST00000352904.5:c.448del
ENST00000412135.6:c.448del
ENST00000440486.6:c.448del
ENST00000481110.6:c.448del
ENST00000613647.4:c.448del
NM_000142.4:c.448del , LRG_1021t1:c.448del
NM_001163213.1:c.448del , LRG_1021t2:c.448del
NM_022965.3:c.448del
XM_006713868.1:c.448del
XM_006713869.1:c.448del
XM_006713870.1:c.448del
XM_006713871.1:c.448del
XM_006713872.1:c.448del
XM_006713873.1:c.448del
XM_011513420.1:c.448del
XM_011513422.1:c.448del
NM_001354809.1:c.448del
NM_001354810.1:c.448del
NR_148971.1:n.704del
NM_001354809.2:c.448del
NM_001354810.2:c.448del
NR_148971.2:n.723del
NM_000142.5:c.448del
NM_001163213.2:c.448del
NM_022965.4:c.448del