Canonical Allele Identifier: CA633167732
Gene: TGFB1 HGNC NCBI
TMEM91 HGNC NCBI

Linked Data

dbSNP Id: rs891302849
gnomAD v2: 19-41859029-T-TG
gnomAD v3: 19-41353124-T-TG
gnomAD v4: 19-41353124-T-TG
MyVariant Identifiers: chr19:g.41859029_41859030insG (hg19) chr19:g.41353124_41353125insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41353129dup , CM000681.2:g.41353129dup GRCh38
NC_000019.9:g.41859034dup , CM000681.1:g.41859034dup GRCh37
NC_000019.8:g.46550874dup NCBI36
NG_013091.1:g.16049dup
NG_013364.1:g.5802dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.-81dup (TGFB1) MANE Select ENSP00000221930.4:n.-81dup
ENST00000221930.5:c.-81dup (TGFB1) ENSP00000221930.4:n.-81dup
ENST00000539627.5:c.-30+1927dup (TMEM91) ENSP00000441900.1:n.-30+1927dup
ENST00000604424.1:n.350+1927dup
NM_000660.5:c.-81dup (TGFB1) NP_000651.3:n.-81dup
XM_011527242.1:c.-81dup (TGFB1) XP_011525544.1:n.-81dup
NM_000660.6:c.-81dup (TGFB1) NP_000651.3:n.-81dup
XM_011527242.2:c.-81dup (TGFB1) XP_011525544.1:n.-81dup
NM_000660.7:c.-81dup (TGFB1) MANE Select NP_000651.3:n.-81dup
Search 100 bp 5'
Search 100 bp 3'