Canonical Allele Identifier: CA344725481
Gene: TGFB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.218520230G>A (hg19) chr1:g.218346888G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346888G>A , CM000663.2:g.218346888G>A GRCh38
NC_000001.10:g.218520230G>A , CM000663.1:g.218520230G>A GRCh37
NC_000001.9:g.216586853G>A NCBI36
NG_027721.1:g.6555G>A
NG_027721.2:g.6555G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.187G>A MANE Select ENSP00000355897.4:p.Val63Ile
ENST00000366929.4:c.187G>A ENSP00000355896.4:p.Val63Ile
ENST00000366930.8:c.187G>A ENSP00000355897.4:p.Val63Ile
NM_001135599.2:c.187G>A NP_001129071.1:p.Val63Ile
NM_003238.3:c.187G>A NP_003229.1:p.Val63Ile
NM_001135599.3:c.187G>A NP_001129071.1:p.Val63Ile
NM_003238.4:c.187G>A NP_003229.1:p.Val63Ile
NR_138148.1:n.1605G>A
NR_138149.1:n.1605G>A
NM_003238.5:c.187G>A NP_003229.1:p.Val63Ile
NM_003238.6:c.187G>A MANE Select NP_003229.1:p.Val63Ile
NM_001135599.4:c.187G>A NP_001129071.1:p.Val63Ile
NR_138148.2:n.1553G>A
NR_138149.2:n.1553G>A
Search 100 bp 5'
Search 100 bp 3'