Canonical Allele Identifier: CA2840836329
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341866C>A , CM000681.2:g.41341866C>A GRCh38
NC_000019.9:g.41847771C>A , CM000681.1:g.41847771C>A GRCh37
NC_000019.8:g.46539611C>A NCBI36
NG_013364.1:g.17061G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.860+17G>T MANE Select ENSP00000221930.4:n.860+17G>T
ENST00000600196.2:c.712+304G>T ENSP00000504008.1:n.712+304G>T
ENST00000677934.1:c.634+2881G>T ENSP00000504769.1:n.634+2881G>T
ENST00000221930.5:c.860+17G>T ENSP00000221930.4:n.860+17G>T
ENST00000598758.5:c.148+17G>T
ENST00000600196.1:n.172+304G>T
NM_000660.5:c.860+17G>T NP_000651.3:n.860+17G>T
XM_011527242.1:c.863+17G>T XP_011525544.1:n.863+17G>T
NM_000660.6:c.860+17G>T NP_000651.3:n.860+17G>T
XM_011527242.2:c.863+17G>T XP_011525544.1:n.863+17G>T
NM_000660.7:c.860+17G>T MANE Select NP_000651.3:n.860+17G>T