Canonical Allele Identifier: CA633470191
Gene: TGFB1 HGNC NCBI

Linked Data

dbSNP Id: rs1336221305

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41332383dup , CM000681.2:g.41332383dup GRCh38
NC_000019.9:g.41838288dup , CM000681.1:g.41838288dup GRCh37
NC_000019.8:g.46530128dup NCBI36
NG_013364.1:g.26550dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.861-96dup MANE Select ENSP00000221930.4:n.861-96dup
ENST00000600196.2:c.713-96dup ENSP00000504008.1:n.713-96dup
ENST00000677934.1:c.635-96dup ENSP00000504769.1:n.635-96dup
ENST00000221930.5:c.861-96dup ENSP00000221930.4:n.861-96dup
ENST00000598758.5:c.149-96dup
ENST00000600196.1:n.173-96dup
NM_000660.5:c.861-96dup NP_000651.3:n.861-96dup
XM_011527242.1:c.864-96dup XP_011525544.1:n.864-96dup
NM_000660.6:c.861-96dup NP_000651.3:n.861-96dup
XM_011527242.2:c.864-96dup XP_011525544.1:n.864-96dup
NM_000660.7:c.861-96dup MANE Select NP_000651.3:n.861-96dup