Canonical Allele Identifier: CA181485050
Gene: GDF6 HGNC NCBI

Linked Data

dbSNP Id: rs532593646
gnomAD v3: 8-96145274-C-T
gnomAD v4: 8-96145274-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96145274C>T , CM000670.2:g.96145274C>T GRCh38
NC_000008.10:g.97157502C>T , CM000670.1:g.97157502C>T GRCh37
NC_000008.9:g.97226678C>T NCBI36
NG_008981.1:g.20519G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287020.7:c.657G>A MANE Select ENSP00000287020.4:p.Gln219=
ENST00000287020.6:c.657G>A ENSP00000287020.4:p.Gln219=
ENST00000620978.1:c.657G>A ENSP00000480170.1:p.Gln219=
ENST00000621429.1:c.657G>A ENSP00000483711.1:p.Gln219=
NM_001001557.2:c.657G>A NP_001001557.1:p.Gln219=
XM_011517030.1:c.258G>A XP_011515332.1:p.Gln86=
NM_001001557.3:c.657G>A NP_001001557.1:p.Gln219=
NM_001001557.4:c.657G>A MANE Select NP_001001557.1:p.Gln219=