Canonical Allele Identifier: CA1804262019
Gene: GDF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96145165G= , CM000670.2:g.96145165G= GRCh38
NC_000008.10:g.97157393G= , CM000670.1:g.97157393G= GRCh37
NC_000008.9:g.97226569G= NCBI36
NG_008981.1:g.20628C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000287020.7:c.766C= MANE Select ENSP00000287020.4:p.Pro256=
ENST00000287020.6:c.766C= ENSP00000287020.4:p.Pro256=
ENST00000620978.1:c.707-3C= ENSP00000480170.1:n.707-3C=
ENST00000621429.1:c.766C= ENSP00000483711.1:p.Pro256=
NM_001001557.2:c.766C= NP_001001557.1:p.Pro256=
XM_011517030.1:c.367C= XP_011515332.1:p.Pro123=
NM_001001557.3:c.766C= NP_001001557.1:p.Pro256=
NM_001001557.4:c.766C= MANE Select NP_001001557.1:p.Pro256=