Canonical Allele Identifier: CA405999736
Gene: TGFB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41847936C>T (hg19) chr19:g.41342031C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342031C>T , CM000681.2:g.41342031C>T GRCh38
NC_000019.9:g.41847936C>T , CM000681.1:g.41847936C>T GRCh37
NC_000019.8:g.46539776C>T NCBI36
NG_013364.1:g.16896G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.713-1G>A MANE Select ENSP00000221930.4:n.713-1G>A
ENST00000600196.2:c.712+139G>A ENSP00000504008.1:n.712+139G>A
ENST00000677934.1:c.634+2716G>A ENSP00000504769.1:n.634+2716G>A
ENST00000221930.5:c.713-1G>A ENSP00000221930.4:n.713-1G>A
ENST00000597453.1:n.382G>A
ENST00000600196.1:n.172+139G>A
NM_000660.5:c.713-1G>A NP_000651.3:n.713-1G>A
XM_011527242.1:c.715G>A XP_011525544.1:p.Gly239Arg
NM_000660.6:c.713-1G>A NP_000651.3:n.713-1G>A
XM_011527242.2:c.715G>A XP_011525544.1:p.Gly239Arg
NM_000660.7:c.713-1G>A MANE Select NP_000651.3:n.713-1G>A
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