Canonical Allele Identifier: CA371751671

Gene: GDF6

Linked Data

• gnomAD v4: 8-96145080-G-T
• MyVariant Identifiers: chr8:g.97157308G>T (hg19) ; chr8:g.96145080G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.96145080G>T , CM000670.2:g.96145080G>T	GRCh38
NC_000008.10:g.97157308G>T , CM000670.1:g.97157308G>T	GRCh37
NC_000008.9:g.97226484G>T	NCBI36
NG_008981.1:g.20713C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000287020.7:c.851C>A MANE Select	ENSP00000287020.4:p.Ser284Tyr
ENST00000287020.6:c.851C>A	ENSP00000287020.4:p.Ser284Tyr
ENST00000620978.1:c.789C>A	ENSP00000480170.1:p.Ile263=
ENST00000621429.1:c.851C>A	ENSP00000483711.1:p.Ser284Tyr
NM_001001557.2:c.851C>A	NP_001001557.1:p.Ser284Tyr
XM_011517030.1:c.452C>A	XP_011515332.1:p.Ser151Tyr
NM_001001557.3:c.851C>A	NP_001001557.1:p.Ser284Tyr
NM_001001557.4:c.851C>A MANE Select	NP_001001557.1:p.Ser284Tyr