Canonical Allele Identifier: CA2585296383
Gene: TGFB1 HGNC NCBI

Linked Data

gnomAD v4: 19-41342144-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342144G>T , CM000681.2:g.41342144G>T GRCh38
NC_000019.9:g.41848049G>T , CM000681.1:g.41848049G>T GRCh37
NC_000019.8:g.46539889G>T NCBI36
NG_013364.1:g.16783C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000221930.6:c.712+26C>A MANE Select ENSP00000221930.4:n.712+26C>A
ENST00000600196.2:c.712+26C>A ENSP00000504008.1:n.712+26C>A
ENST00000677934.1:c.634+2603C>A ENSP00000504769.1:n.634+2603C>A
ENST00000221930.5:c.712+26C>A ENSP00000221930.4:n.712+26C>A
ENST00000597453.1:n.269C>A
ENST00000600196.1:n.172+26C>A
NM_000660.5:c.712+26C>A NP_000651.3:n.712+26C>A
XM_011527242.1:c.712+26C>A XP_011525544.1:n.712+26C>A
NM_000660.6:c.712+26C>A NP_000651.3:n.712+26C>A
XM_011527242.2:c.712+26C>A XP_011525544.1:n.712+26C>A
NM_000660.7:c.712+26C>A MANE Select NP_000651.3:n.712+26C>A
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