Canonical Allele Identifier: CA462454878
Gene: GDF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.97157484G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96145256G>T , CM000670.2:g.96145256G>T GRCh38
NC_000008.10:g.97157484G>T , CM000670.1:g.97157484G>T GRCh37
NC_000008.9:g.97226660G>T NCBI36
NG_008981.1:g.20537C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287020.7:c.675C>A MANE Select ENSP00000287020.4:p.Pro225=
ENST00000287020.6:c.675C>A ENSP00000287020.4:p.Pro225=
ENST00000620978.1:c.675C>A ENSP00000480170.1:p.Pro225=
ENST00000621429.1:c.675C>A ENSP00000483711.1:p.Pro225=
NM_001001557.2:c.675C>A NP_001001557.1:p.Pro225=
XM_011517030.1:c.276C>A XP_011515332.1:p.Pro92=
NM_001001557.3:c.675C>A NP_001001557.1:p.Pro225=
NM_001001557.4:c.675C>A MANE Select NP_001001557.1:p.Pro225=