Canonical Allele Identifier: CA462454792
Gene: GDF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.97172546A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96160318A>G , CM000670.2:g.96160318A>G GRCh38
NC_000008.10:g.97172546A>G , CM000670.1:g.97172546A>G GRCh37
NC_000008.9:g.97241722A>G NCBI36
NG_008981.1:g.5475T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287020.7:c.375T>C MANE Select ENSP00000287020.4:p.Asn125=
ENST00000287020.6:c.375T>C ENSP00000287020.4:p.Asn125=
ENST00000620978.1:c.375T>C ENSP00000480170.1:p.Asn125=
ENST00000621429.1:c.375T>C ENSP00000483711.1:p.Asn125=
NM_001001557.2:c.375T>C NP_001001557.1:p.Asn125=
NM_001001557.3:c.375T>C NP_001001557.1:p.Asn125=
NM_001001557.4:c.375T>C MANE Select NP_001001557.1:p.Asn125=
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