Canonical Allele Identifier: CA2698070446
Gene: TGFB2 HGNC NCBI

Linked Data

dbSNP Id: rs2102629933

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218437336_218437337insAAAA , CM000663.2:g.218437336_218437337insAAAA GRCh38
NC_000001.10:g.218610678_218610679insAAAA , CM000663.1:g.218610678_218610679insAAAA GRCh37
NC_000001.9:g.216677301_216677302insAAAA NCBI36
NG_027721.1:g.97003_97004insAAAA
NG_027721.2:g.97003_97004insAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000366930.9:c.933-7_933-6insAAAA MANE Select ENSP00000355897.4:n.933-7_933-6insAAAA
ENST00000366929.4:c.1017-7_1017-6insAAAA ENSP00000355896.4:n.1017-7_1017-6insAAAA
ENST00000366930.8:c.933-7_933-6insAAAA ENSP00000355897.4:n.933-7_933-6insAAAA
ENST00000479322.1:n.417-7_417-6insAAAA
NM_001135599.2:c.1017-7_1017-6insAAAA NP_001129071.1:n.1017-7_1017-6insAAAA
NM_003238.3:c.933-7_933-6insAAAA NP_003229.1:n.933-7_933-6insAAAA
NM_001135599.3:c.1017-7_1017-6insAAAA NP_001129071.1:n.1017-7_1017-6insAAAA
NM_003238.4:c.933-7_933-6insAAAA NP_003229.1:n.933-7_933-6insAAAA
NR_138148.1:n.2236-7_2236-6insAAAA
NR_138149.1:n.2320-7_2320-6insAAAA
NM_003238.5:c.933-7_933-6insAAAA NP_003229.1:n.933-7_933-6insAAAA
NM_003238.6:c.933-7_933-6insAAAA MANE Select NP_003229.1:n.933-7_933-6insAAAA
NM_001135599.4:c.1017-7_1017-6insAAAA NP_001129071.1:n.1017-7_1017-6insAAAA
NR_138148.2:n.2184-7_2184-6insAAAA
NR_138149.2:n.2268-7_2268-6insAAAA