Canonical Allele Identifier: CA1116871900

Gene: GDF6

Linked Data

• dbSNP Id: rs1812736866
• gnomAD v3: 8-96160229-G-GCTCC
• gnomAD v4: 8-96160229-G-GCTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.96160232_96160235dup , CM000670.2:g.96160232_96160235dup	GRCh38
NC_000008.10:g.97172460_97172463dup , CM000670.1:g.97172460_97172463dup	GRCh37
NC_000008.9:g.97241636_97241639dup	NCBI36
NG_008981.1:g.5560_5563dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287020.7:c.406+54_406+57dup MANE Select	ENSP00000287020.4:n.406+54_406+57dup
ENST00000287020.6:c.406+54_406+57dup	ENSP00000287020.4:n.406+54_406+57dup
ENST00000620978.1:c.406+54_406+57dup	ENSP00000480170.1:n.406+54_406+57dup
ENST00000621429.1:c.406+54_406+57dup	ENSP00000483711.1:n.406+54_406+57dup
NM_001001557.2:c.406+54_406+57dup	NP_001001557.1:n.406+54_406+57dup
NM_001001557.3:c.406+54_406+57dup	NP_001001557.1:n.406+54_406+57dup
NM_001001557.4:c.406+54_406+57dup MANE Select	NP_001001557.1:n.406+54_406+57dup