Canonical Allele Identifier: CA462454602
Gene: GDF6 HGNC NCBI

Linked Data

gnomAD v4: 8-96145184-C-T
MyVariant Identifiers: chr8:g.97157412C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96145184C>T , CM000670.2:g.96145184C>T GRCh38
NC_000008.10:g.97157412C>T , CM000670.1:g.97157412C>T GRCh37
NC_000008.9:g.97226588C>T NCBI36
NG_008981.1:g.20609G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287020.7:c.747G>A MANE Select ENSP00000287020.4:p.Ala249=
ENST00000287020.6:c.747G>A ENSP00000287020.4:p.Ala249=
ENST00000620978.1:c.707-22G>A ENSP00000480170.1:n.707-22G>A
ENST00000621429.1:c.747G>A ENSP00000483711.1:p.Ala249=
NM_001001557.2:c.747G>A NP_001001557.1:p.Ala249=
XM_011517030.1:c.348G>A XP_011515332.1:p.Ala116=
NM_001001557.3:c.747G>A NP_001001557.1:p.Ala249=
NM_001001557.4:c.747G>A MANE Select NP_001001557.1:p.Ala249=