LDH info

Canonical Allele Identifier: CA2810002
Gene: FGFR3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 255346
dbSNP Id: rs2234909

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1801977T>C , CM000666.2:g.1801977T>C GRCh38
NC_000004.11:g.1803704T>C , CM000666.1:g.1803704T>C GRCh37
NC_000004.10:g.1773502T>C NCBI36
NG_012632.1:g.13666T>C , LRG_1021:g.13666T>C

Transcript Alleles

HGVS Amino-acid change
NM_000142.4:c.882T>C , LRG_1021t1:c.882T>C NP_000133.1:p.Asn294=
NM_001163213.1:c.882T>C , LRG_1021t2:c.882T>C NP_001156685.1:p.Asn294=
NM_022965.3:c.882T>C VV NP_075254.1:p.Asn294=
XM_006713868.1:c.882T>C XP_006713931.1:p.Asn294=
XM_006713869.1:c.882T>C XP_006713932.1:p.Asn294=
XM_006713870.1:c.882T>C XP_006713933.1:p.Asn294=
XM_006713871.1:c.882T>C XP_006713934.1:p.Asn294=
XM_006713872.1:c.882T>C XP_006713935.1:p.Asn294=
XM_006713873.1:c.882T>C XP_006713936.1:p.Asn294=
XM_011513420.1:c.882T>C XP_011511722.1:p.Asn294=
XM_011513422.1:c.882T>C XP_011511724.1:p.Asn294=
NM_001354809.1:c.882T>C VV NP_001341738.1:p.Asn294=
NM_001354810.1:c.882T>C VV NP_001341739.1:p.Asn294=
NR_148971.1:n.1138T>C
NM_001354809.2:c.882T>C VV NP_001341738.1:p.Asn294=
NM_001354810.2:c.882T>C VV NP_001341739.1:p.Asn294=
NR_148971.2:n.1157T>C
ENST00000260795.6:c.882T>C ENSP00000260795.2:p.Asn294=
ENST00000340107.8:c.882T>C ENSP00000339824.4:p.Asn294=
ENST00000352904.5:c.882T>C ENSP00000231803.1:p.Asn294=
ENST00000412135.6:c.882T>C ENSP00000412903.2:p.Asn294=
ENST00000440486.6:c.882T>C ENSP00000414914.2:p.Asn294=
ENST00000474521.1:n.258T>C
ENST00000481110.6:c.882T>C ENSP00000420533.2:p.Asn294=
ENST00000507588.1:n.288+54T>C ENSP00000427289.1:p.=
ENST00000613647.4:c.882T>C ENSP00000479472.1:p.Asn294=