Canonical Allele Identifier: CA469780883

Gene: GDF2

Linked Data

• gnomAD v4: 10-47325220-C-T
• MyVariant Identifiers: chr10:g.48414142G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.47325220C>T , CM000672.2:g.47325220C>T	GRCh38
NC_000010.10:g.48414142G>A , CM000672.1:g.48414142G>A	GRCh37
NC_000010.9:g.48034148G>A	NCBI36
NG_033916.1:g.7731C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581492.3:c.726C>T MANE Select	ENSP00000463051.1:p.Ile242=
ENST00000581492.2:c.726C>T	ENSP00000463051.1:p.Ile242=
NM_016204.2:c.726C>T	NP_057288.1:p.Ile242=
XM_006717761.2:c.726C>T	XP_006717824.1:p.Ile242=
NM_016204.3:c.726C>T	NP_057288.1:p.Ile242=
NM_016204.4:c.726C>T MANE Select	NP_057288.1:p.Ile242=