Canonical Allele Identifier: CA37619334

Gene: TGFB2

Linked Data

• dbSNP Id: rs776899072
• gnomAD v4: 1-218434273-A-G
• MyVariant Identifiers: chr1:g.218607615A>G (hg19) ; chr1:g.218434273A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218434273A>G , CM000663.2:g.218434273A>G	GRCh38
NC_000001.10:g.218607615A>G , CM000663.1:g.218607615A>G	GRCh37
NC_000001.9:g.216674238A>G	NCBI36
NG_027721.1:g.93940A>G
NG_027721.2:g.93940A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.643+59A>G MANE Select	ENSP00000355897.4:n.643+59A>G
ENST00000366929.4:c.727+59A>G	ENSP00000355896.4:n.727+59A>G
ENST00000366930.8:c.643+59A>G	ENSP00000355897.4:n.643+59A>G
ENST00000479322.1:n.127+21A>G
ENST00000488793.1:n.366A>G
NM_001135599.2:c.727+59A>G	NP_001129071.1:n.727+59A>G
NM_003238.3:c.643+59A>G	NP_003229.1:n.643+59A>G
NM_001135599.3:c.727+59A>G	NP_001129071.1:n.727+59A>G
NM_003238.4:c.643+59A>G	NP_003229.1:n.643+59A>G
NR_138148.1:n.2061+59A>G
NR_138149.1:n.2145+59A>G
NM_003238.5:c.643+59A>G	NP_003229.1:n.643+59A>G
NM_003238.6:c.643+59A>G MANE Select	NP_003229.1:n.643+59A>G
NM_001135599.4:c.727+59A>G	NP_001129071.1:n.727+59A>G
NR_138148.2:n.2009+59A>G
NR_138149.2:n.2093+59A>G