Canonical Allele Identifier: CA406003648
Gene: TGFB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41348371G>C , CM000681.2:g.41348371G>C GRCh38
NC_000019.9:g.41854276G>C , CM000681.1:g.41854276G>C GRCh37
NC_000019.8:g.46546116G>C NCBI36
NG_013364.1:g.10556C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.440C>G MANE Select ENSP00000221930.4:p.Pro147Arg
ENST00000600196.2:c.440C>G ENSP00000504008.1:p.Pro147Arg
ENST00000677934.1:c.440C>G ENSP00000504769.1:p.Pro147Arg
ENST00000221930.5:c.440C>G ENSP00000221930.4:p.Pro147Arg
NM_000660.5:c.440C>G NP_000651.3:p.Pro147Arg
XM_011527242.1:c.440C>G XP_011525544.1:p.Pro147Arg
NM_000660.6:c.440C>G NP_000651.3:p.Pro147Arg
XM_011527242.2:c.440C>G XP_011525544.1:p.Pro147Arg
NM_000660.7:c.440C>G MANE Select NP_000651.3:p.Pro147Arg