Canonical Allele Identifier: CA462454618
Gene: GDF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.97157421C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96145193C>T , CM000670.2:g.96145193C>T GRCh38
NC_000008.10:g.97157421C>T , CM000670.1:g.97157421C>T GRCh37
NC_000008.9:g.97226597C>T NCBI36
NG_008981.1:g.20600G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287020.7:c.738G>A MANE Select ENSP00000287020.4:p.Glu246=
ENST00000287020.6:c.738G>A ENSP00000287020.4:p.Glu246=
ENST00000620978.1:c.707-31G>A ENSP00000480170.1:n.707-31G>A
ENST00000621429.1:c.738G>A ENSP00000483711.1:p.Glu246=
NM_001001557.2:c.738G>A NP_001001557.1:p.Glu246=
XM_011517030.1:c.339G>A XP_011515332.1:p.Glu113=
NM_001001557.3:c.738G>A NP_001001557.1:p.Glu246=
NM_001001557.4:c.738G>A MANE Select NP_001001557.1:p.Glu246=