LDH info

Canonical Allele Identifier: CA15320073
Gene: FGFR3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3135848

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1796014T>C , CM000666.2:g.1796014T>C GRCh38
NC_000004.11:g.1797741T>C , CM000666.1:g.1797741T>C GRCh37
NC_000004.10:g.1767539T>C NCBI36
NG_012632.1:g.7703T>C , LRG_1021:g.7703T>C

Transcript Alleles

HGVS Amino-acid change
NM_000142.4:c.109+1971T>C , LRG_1021t1:c.109+1971T>C NP_000133.1:p.=
NM_001163213.1:c.109+1971T>C , LRG_1021t2:c.109+1971T>C NP_001156685.1:p.=
NM_022965.3:c.109+1971T>C VV NP_075254.1:p.=
XM_006713868.1:c.109+1971T>C XP_006713931.1:p.=
XM_006713869.1:c.109+1971T>C XP_006713932.1:p.=
XM_006713870.1:c.109+1971T>C XP_006713933.1:p.=
XM_006713871.1:c.109+1971T>C XP_006713934.1:p.=
XM_006713872.1:c.109+1971T>C XP_006713935.1:p.=
XM_006713873.1:c.109+1971T>C XP_006713936.1:p.=
XM_011513420.1:c.109+1971T>C XP_011511722.1:p.=
XM_011513422.1:c.109+1971T>C XP_011511724.1:p.=
NM_001354809.1:c.109+1971T>C VV NP_001341738.1:p.=
NM_001354810.1:c.109+1971T>C VV NP_001341739.1:p.=
NR_148971.1:n.365+1971T>C
NM_001354809.2:c.109+1971T>C VV NP_001341738.1:p.=
NM_001354810.2:c.109+1971T>C VV NP_001341739.1:p.=
NR_148971.2:n.384+1971T>C
ENST00000260795.6:c.109+1971T>C ENSP00000260795.2:p.=
ENST00000340107.8:c.109+1971T>C ENSP00000339824.4:p.=
ENST00000352904.5:c.109+1971T>C ENSP00000231803.1:p.=
ENST00000412135.6:c.109+1971T>C ENSP00000412903.2:p.=
ENST00000440486.6:c.109+1971T>C ENSP00000414914.2:p.=
ENST00000481110.6:c.109+1971T>C ENSP00000420533.2:p.=
ENST00000613647.4:c.109+1971T>C ENSP00000479472.1:p.=