Canonical Allele Identifier: CA4815526
Gene: GDF6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1136022
ClinVar RCV Id: RCV001471537
dbSNP Id: rs763584976
gnomAD v2: 8-97172696-G-A
gnomAD v3: 8-96160468-G-A
gnomAD v4: 8-96160468-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96160468G>A , CM000670.2:g.96160468G>A GRCh38
NC_000008.10:g.97172696G>A , CM000670.1:g.97172696G>A GRCh37
NC_000008.9:g.97241872G>A NCBI36
NG_008981.1:g.5325C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000287020.7:c.225C>T MANE Select ENSP00000287020.4:p.Pro75=
ENST00000287020.6:c.225C>T ENSP00000287020.4:p.Pro75=
ENST00000620978.1:c.225C>T ENSP00000480170.1:p.Pro75=
ENST00000621429.1:c.225C>T ENSP00000483711.1:p.Pro75=
NM_001001557.2:c.225C>T NP_001001557.1:p.Pro75=
NM_001001557.3:c.225C>T NP_001001557.1:p.Pro75=
NM_001001557.4:c.225C>T MANE Select NP_001001557.1:p.Pro75=