Canonical Allele Identifier: CA314131800
Gene: GDF5 HGNC NCBI

Linked Data

dbSNP Id: rs888922065

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35438137C>T , CM000682.2:g.35438137C>T GRCh38
NC_000020.10:g.34025917C>T , CM000682.1:g.34025917C>T GRCh37
NC_000020.9:g.33489331C>T NCBI36
NG_008076.2:g.5083G>A
NG_008076.3:g.21610G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374369.8:c.-209G>A MANE Select ENSP00000363489.3:n.-209G>A
ENST00000374369.7:c.-209G>A ENSP00000363489.3:n.-209G>A
ENST00000374372.1:c.-209G>A ENSP00000363492.1:n.-209G>A
NM_000557.4:c.-209G>A NP_000548.2:n.-209G>A
XM_011529075.1:c.-209G>A XP_011527377.1:n.-209G>A
XM_011529076.1:c.-209G>A XP_011527378.1:n.-209G>A
NM_001319138.1:c.-209G>A NP_001306067.1:n.-209G>A
NM_000557.5:c.-209G>A MANE Select NP_000548.2:n.-209G>A
NM_001319138.2:c.-209G>A NP_001306067.1:n.-209G>A