Canonical Allele Identifier: CA1276622000
Gene: TGFBRAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.105261413C= , CM000664.2:g.105261413C= GRCh38
NC_000002.11:g.105877870C= , CM000664.1:g.105877870C= GRCh37
NC_000002.10:g.105244302C= NCBI36
NG_050952.1:g.73302G=

Transcript Alleles

HGVS Amino-acid Change
XM_011512193.1:c.2406+7859G= XP_011510495.1:n.2406+7859G=
NM_001328646.1:c.2406+7859G= NP_001315575.1:n.2406+7859G=
NM_001328646.2:c.2406+7859G= NP_001315575.1:n.2406+7859G=
NM_001328646.3:c.2406+7859G= NP_001315575.1:n.2406+7859G=