Canonical Allele Identifier: CA906173036

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1163714164
• gnomAD v3: 3-30606490-G-A
• gnomAD v4: 3-30606490-G-A
• MyVariant Identifiers: chr3:g.30647982G>A (hg19) ; chr3:g.30606490G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30606490G>A , CM000665.2:g.30606490G>A	GRCh38
NC_000003.11:g.30647982G>A , CM000665.1:g.30647982G>A	GRCh37
NC_000003.10:g.30622986G>A	NCBI36
NG_007490.1:g.4989G>A , LRG_779:g.4989G>A

Transcript Alleles

HGVS	Amino-acid Change
XM_011534045.3:c.-115G>A	XP_011532347.1:n.-115G>A