LDH info

Canonical Allele Identifier: CA13206526
Gene: FGFR2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3135718

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121594355C>T , CM000672.2:g.121594355C>T GRCh38
NC_000010.10:g.123353869C>T , CM000672.1:g.123353869C>T GRCh37
NC_000010.9:g.123343859C>T NCBI36
NG_012449.1:g.9104G>A
NG_012449.2:g.9104G>A

Transcript Alleles

HGVS Amino-acid change
NM_000141.4:c.-150-388G>A VV NP_000132.3:p.=
NM_001144915.1:c.-150-388G>A VV NP_001138387.1:p.=
NM_001144917.1:c.-150-388G>A VV NP_001138389.1:p.=
NM_001144918.1:c.-150-388G>A VV NP_001138390.1:p.=
NM_001144919.1:c.-150-388G>A VV NP_001138391.1:p.=
NM_022970.3:c.-150-388G>A VV NP_075259.4:p.=
NR_073009.1:n.498-388G>A
XM_006717708.2:c.-93-388G>A XP_006717771.1:p.=
XM_006717709.2:c.-93-388G>A XP_006717772.1:p.=
XM_006717710.2:c.-93-388G>A XP_006717773.1:p.=
XM_006717713.2:c.-93-388G>A XP_006717776.1:p.=
NM_001320658.1:c.-150-388G>A VV NP_001307587.1:p.=
XM_006717708.3:c.-93-388G>A XP_006717771.1:p.=
XM_006717710.4:c.-93-388G>A XP_006717773.1:p.=
XM_017015920.2:c.-93-388G>A XP_016871409.1:p.=
XM_017015921.2:c.-93-388G>A XP_016871410.1:p.=
XM_017015924.2:c.-93-388G>A XP_016871413.1:p.=
XM_017015925.2:c.-93-388G>A XP_016871414.1:p.=
XM_024447887.1:c.-93-388G>A XP_024303655.1:p.=
XM_024447888.1:c.-93-388G>A XP_024303656.1:p.=
XM_024447889.1:c.-93-388G>A XP_024303657.1:p.=
XM_024447890.1:c.-93-388G>A XP_024303658.1:p.=
XM_024447891.1:c.-93-388G>A XP_024303659.1:p.=
ENST00000336553.10:c.-150-388G>A ENSP00000337665.6:p.=
ENST00000356226.8:c.-150-388G>A ENSP00000348559.4:p.=
ENST00000357555.9:c.-150-388G>A ENSP00000350166.5:p.=
ENST00000358487.9:c.-150-388G>A ENSP00000351276.5:p.=
ENST00000359354.6:c.-150-388G>A ENSP00000352309.2:p.=
ENST00000360144.7:c.-150-388G>A ENSP00000353262.3:p.=
ENST00000369058.7:c.-150-388G>A ENSP00000358054.3:p.=
ENST00000369059.5:c.-150-388G>A ENSP00000358055.1:p.=
ENST00000369060.8:c.-150-388G>A ENSP00000358056.4:p.=
ENST00000457416.6:c.-150-388G>A ENSP00000410294.2:p.=
ENST00000490349.5:n.112-388G>A
ENST00000604236.5:c.-150-388G>A ENSP00000474109.1:p.=
ENST00000613048.4:c.-150-388G>A ENSP00000484154.1:p.=