Canonical Allele Identifier: CA462454914
Gene: GDF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.97157496C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96145268C>G , CM000670.2:g.96145268C>G GRCh38
NC_000008.10:g.97157496C>G , CM000670.1:g.97157496C>G GRCh37
NC_000008.9:g.97226672C>G NCBI36
NG_008981.1:g.20525G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287020.7:c.663G>C MANE Select ENSP00000287020.4:p.Leu221=
ENST00000287020.6:c.663G>C ENSP00000287020.4:p.Leu221=
ENST00000620978.1:c.663G>C ENSP00000480170.1:p.Leu221=
ENST00000621429.1:c.663G>C ENSP00000483711.1:p.Leu221=
NM_001001557.2:c.663G>C NP_001001557.1:p.Leu221=
XM_011517030.1:c.264G>C XP_011515332.1:p.Leu88=
NM_001001557.3:c.663G>C NP_001001557.1:p.Leu221=
NM_001001557.4:c.663G>C MANE Select NP_001001557.1:p.Leu221=