Canonical Allele Identifier: CA462454662
Gene: GDF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.97172713G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96160485G>T , CM000670.2:g.96160485G>T GRCh38
NC_000008.10:g.97172713G>T , CM000670.1:g.97172713G>T GRCh37
NC_000008.9:g.97241889G>T NCBI36
NG_008981.1:g.5308C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287020.7:c.208C>A MANE Select ENSP00000287020.4:p.Arg70=
ENST00000287020.6:c.208C>A ENSP00000287020.4:p.Arg70=
ENST00000620978.1:c.208C>A ENSP00000480170.1:p.Arg70=
ENST00000621429.1:c.208C>A ENSP00000483711.1:p.Arg70=
NM_001001557.2:c.208C>A NP_001001557.1:p.Arg70=
NM_001001557.3:c.208C>A NP_001001557.1:p.Arg70=
NM_001001557.4:c.208C>A MANE Select NP_001001557.1:p.Arg70=