Canonical Allele Identifier: CA371751811

Gene: GDF6

Linked Data

• gnomAD v4: 8-96145130-C-G
• COSMIC: COSM51106
• MyVariant Identifiers: chr8:g.97157358C>G (hg19) ; chr8:g.96145130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.96145130C>G , CM000670.2:g.96145130C>G	GRCh38
NC_000008.10:g.97157358C>G , CM000670.1:g.97157358C>G	GRCh37
NC_000008.9:g.97226534C>G	NCBI36
NG_008981.1:g.20663G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287020.7:c.801G>C MANE Select	ENSP00000287020.4:p.Arg267=
ENST00000287020.6:c.801G>C	ENSP00000287020.4:p.Arg267=
ENST00000620978.1:c.739G>C	ENSP00000480170.1:p.Glu247Gln
ENST00000621429.1:c.801G>C	ENSP00000483711.1:p.Arg267=
NM_001001557.2:c.801G>C	NP_001001557.1:p.Arg267=
XM_011517030.1:c.402G>C	XP_011515332.1:p.Arg134=
NM_001001557.3:c.801G>C	NP_001001557.1:p.Arg267=
NM_001001557.4:c.801G>C MANE Select	NP_001001557.1:p.Arg267=