Canonical Allele Identifier: CA406003565
Gene: TGFB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41348325T>G , CM000681.2:g.41348325T>G GRCh38
NC_000019.9:g.41854230T>G , CM000681.1:g.41854230T>G GRCh37
NC_000019.8:g.46546070T>G NCBI36
NG_013364.1:g.10602A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.486A>C MANE Select ENSP00000221930.4:p.Leu162Phe
ENST00000600196.2:c.486A>C ENSP00000504008.1:p.Leu162Phe
ENST00000677934.1:c.486A>C ENSP00000504769.1:p.Leu162Phe
ENST00000221930.5:c.486A>C ENSP00000221930.4:p.Leu162Phe
ENST00000597453.1:n.17A>C
NM_000660.5:c.486A>C NP_000651.3:p.Leu162Phe
XM_011527242.1:c.486A>C XP_011525544.1:p.Leu162Phe
NM_000660.6:c.486A>C NP_000651.3:p.Leu162Phe
XM_011527242.2:c.486A>C XP_011525544.1:p.Leu162Phe
NM_000660.7:c.486A>C MANE Select NP_000651.3:p.Leu162Phe