Canonical Allele Identifier: CA314131794

Gene: GDF5

Linked Data

• dbSNP Id: rs925696155
• gnomAD v2: 20-34025876-C-T
• gnomAD v3: 20-35438096-C-T
• gnomAD v4: 20-35438096-C-T
• MyVariant Identifiers: chr20:g.34025876C>T (hg19) ; chr20:g.35438096C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35438096C>T , CM000682.2:g.35438096C>T	GRCh38
NC_000020.10:g.34025876C>T , CM000682.1:g.34025876C>T	GRCh37
NC_000020.9:g.33489290C>T	NCBI36
NG_008076.2:g.5124G>A
NG_008076.3:g.21651G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374369.8:c.-168G>A MANE Select	ENSP00000363489.3:n.-168G>A
ENST00000374369.7:c.-168G>A	ENSP00000363489.3:n.-168G>A
ENST00000374372.1:c.-168G>A	ENSP00000363492.1:n.-168G>A
NM_000557.4:c.-168G>A	NP_000548.2:n.-168G>A
XM_011529075.1:c.-168G>A	XP_011527377.1:n.-168G>A
XM_011529076.1:c.-168G>A	XP_011527378.1:n.-168G>A
NM_001319138.1:c.-168G>A	NP_001306067.1:n.-168G>A
NM_000557.5:c.-168G>A MANE Select	NP_000548.2:n.-168G>A
NM_001319138.2:c.-168G>A	NP_001306067.1:n.-168G>A