Canonical Allele Identifier: CA462454816
Gene: GDF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.97157265G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96145037G>C , CM000670.2:g.96145037G>C GRCh38
NC_000008.10:g.97157265G>C , CM000670.1:g.97157265G>C GRCh37
NC_000008.9:g.97226441G>C NCBI36
NG_008981.1:g.20756C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287020.7:c.894C>G MANE Select ENSP00000287020.4:p.Gly298=
ENST00000287020.6:c.894C>G ENSP00000287020.4:p.Gly298=
ENST00000620978.1:c.793+39C>G ENSP00000480170.1:n.793+39C>G
ENST00000621429.1:c.874+20C>G ENSP00000483711.1:n.874+20C>G
NM_001001557.2:c.894C>G NP_001001557.1:p.Gly298=
XM_011517030.1:c.495C>G XP_011515332.1:p.Gly165=
NM_001001557.3:c.894C>G NP_001001557.1:p.Gly298=
NM_001001557.4:c.894C>G MANE Select NP_001001557.1:p.Gly298=
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