Canonical Allele Identifier: CA37622239

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437380A>G , CM000663.2:g.218437380A>G	GRCh38
NC_000001.10:g.218610722A>G , CM000663.1:g.218610722A>G	GRCh37
NC_000001.9:g.216677345A>G	NCBI36
NG_027721.1:g.97047A>G
NG_027721.2:g.97047A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.970A>G MANE Select	ENSP00000355897.4:p.Ile324Val
ENST00000366929.4:c.1054A>G	ENSP00000355896.4:p.Ile352Val
ENST00000366930.8:c.970A>G	ENSP00000355897.4:p.Ile324Val
ENST00000479322.1:n.454A>G
NM_001135599.2:c.1054A>G	NP_001129071.1:p.Ile352Val
NM_003238.3:c.970A>G	NP_003229.1:p.Ile324Val
NM_001135599.3:c.1054A>G	NP_001129071.1:p.Ile352Val
NM_003238.4:c.970A>G	NP_003229.1:p.Ile324Val
NR_138148.1:n.2273A>G
NR_138149.1:n.2357A>G
NM_003238.5:c.970A>G	NP_003229.1:p.Ile324Val
NM_003238.6:c.970A>G MANE Select	NP_003229.1:p.Ile324Val
NM_001135599.4:c.1054A>G	NP_001129071.1:p.Ile352Val
NR_138148.2:n.2221A>G
NR_138149.2:n.2305A>G