Canonical Allele Identifier: CA731608689

Gene: TGFB2

Linked Data

• dbSNP Id: rs1411474013
• MyVariant Identifiers: chr1:g.218610619G>C (hg19) ; chr1:g.218437277G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437277G>C , CM000663.2:g.218437277G>C	GRCh38
NC_000001.10:g.218610619G>C , CM000663.1:g.218610619G>C	GRCh37
NC_000001.9:g.216677242G>C	NCBI36
NG_027721.1:g.96944G>C
NG_027721.2:g.96944G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.933-66G>C MANE Select	ENSP00000355897.4:n.933-66G>C
ENST00000366929.4:c.1017-66G>C	ENSP00000355896.4:n.1017-66G>C
ENST00000366930.8:c.933-66G>C	ENSP00000355897.4:n.933-66G>C
ENST00000479322.1:n.417-66G>C
NM_001135599.2:c.1017-66G>C	NP_001129071.1:n.1017-66G>C
NM_003238.3:c.933-66G>C	NP_003229.1:n.933-66G>C
NM_001135599.3:c.1017-66G>C	NP_001129071.1:n.1017-66G>C
NM_003238.4:c.933-66G>C	NP_003229.1:n.933-66G>C
NR_138148.1:n.2236-66G>C
NR_138149.1:n.2320-66G>C
NM_003238.5:c.933-66G>C	NP_003229.1:n.933-66G>C
NM_003238.6:c.933-66G>C MANE Select	NP_003229.1:n.933-66G>C
NM_001135599.4:c.1017-66G>C	NP_001129071.1:n.1017-66G>C
NR_138148.2:n.2184-66G>C
NR_138149.2:n.2268-66G>C