Canonical Allele Identifier: CA37543368

Gene: TGFB2

Linked Data

• dbSNP Id: rs898159874
• gnomAD v4: 1-218345710-G-T
• MyVariant Identifiers: chr1:g.218519052G>T (hg19) ; chr1:g.218345710G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218345710G>T , CM000663.2:g.218345710G>T	GRCh38
NC_000001.10:g.218519052G>T , CM000663.1:g.218519052G>T	GRCh37
NC_000001.9:g.216585675G>T	NCBI36
NG_027721.1:g.5377G>T
NG_027721.2:g.5377G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-992G>T MANE Select	ENSP00000355897.4:n.-992G>T
NM_001135599.2:c.-992G>T	NP_001129071.1:n.-992G>T
NM_003238.3:c.-992G>T	NP_003229.1:n.-992G>T
NM_001135599.3:c.-992G>T	NP_001129071.1:n.-992G>T
NM_003238.4:c.-992G>T	NP_003229.1:n.-992G>T
NR_138148.1:n.427G>T
NR_138149.1:n.427G>T
NM_003238.5:c.-992G>T	NP_003229.1:n.-992G>T
NM_003238.6:c.-992G>T MANE Select	NP_003229.1:n.-992G>T
NM_001135599.4:c.-992G>T	NP_001129071.1:n.-992G>T
NR_138148.2:n.375G>T
NR_138149.2:n.375G>T