Canonical Allele Identifier: CA2650531906
Gene: TGFB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218437337_218437338insC , CM000663.2:g.218437337_218437338insC GRCh38
NC_000001.10:g.218610679_218610680insC , CM000663.1:g.218610679_218610680insC GRCh37
NC_000001.9:g.216677302_216677303insC NCBI36
NG_027721.1:g.97004_97005insC
NG_027721.2:g.97004_97005insC

Transcript Alleles

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