Canonical Allele Identifier: CA119556
Gene: GDF6 HGNC NCBI

Linked Data

ClinVar Variation Id: 8372
dbSNP Id: rs63751220
gnomAD v2: 8-97157293-A-G
gnomAD v3: 8-96145065-A-G
gnomAD v4: 8-96145065-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96145065A>G , CM000670.2:g.96145065A>G GRCh38
NC_000008.10:g.97157293A>G , CM000670.1:g.97157293A>G GRCh37
NC_000008.9:g.97226469A>G NCBI36
NG_008981.1:g.20728T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287020.7:c.866T>C MANE Select ENSP00000287020.4:p.Leu289Pro
ENST00000287020.6:c.866T>C ENSP00000287020.4:p.Leu289Pro
ENST00000620978.1:c.793+11T>C ENSP00000480170.1:n.793+11T>C
ENST00000621429.1:c.866T>C ENSP00000483711.1:p.Leu289Pro
NM_001001557.2:c.866T>C NP_001001557.1:p.Leu289Pro
XM_011517030.1:c.467T>C XP_011515332.1:p.Leu156Pro
NM_001001557.3:c.866T>C NP_001001557.1:p.Leu289Pro
NM_001001557.4:c.866T>C MANE Select NP_001001557.1:p.Leu289Pro