Canonical Allele Identifier: CA469780897
Gene: GDF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48414133G>T (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000581492.3:c.735C>A MANE Select ENSP00000463051.1:p.Pro245=
ENST00000581492.2:c.735C>A ENSP00000463051.1:p.Pro245=
NM_016204.2:c.735C>A NP_057288.1:p.Pro245=
XM_006717761.2:c.735C>A XP_006717824.1:p.Pro245=
NM_016204.3:c.735C>A NP_057288.1:p.Pro245=
NM_016204.4:c.735C>A MANE Select NP_057288.1:p.Pro245=
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Search 100 bp 3'