Canonical Allele Identifier: CA469780895

Gene: GDF2

Linked Data

• MyVariant Identifiers: chr10:g.48414133G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.47325229C>G , CM000672.2:g.47325229C>G	GRCh38
NC_000010.10:g.48414133G>C , CM000672.1:g.48414133G>C	GRCh37
NC_000010.9:g.48034139G>C	NCBI36
NG_033916.1:g.7740C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581492.3:c.735C>G MANE Select	ENSP00000463051.1:p.Pro245=
ENST00000581492.2:c.735C>G	ENSP00000463051.1:p.Pro245=
NM_016204.2:c.735C>G	NP_057288.1:p.Pro245=
XM_006717761.2:c.735C>G	XP_006717824.1:p.Pro245=
NM_016204.3:c.735C>G	NP_057288.1:p.Pro245=
NM_016204.4:c.735C>G MANE Select	NP_057288.1:p.Pro245=