Canonical Allele Identifier: CA913102721
Gene: TGFBR2 HGNC NCBI

Linked Data

gnomAD v4: 3-30606881-G-T
MyVariant Identifiers: chr3:g.30648373G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606881G>T , CM000665.2:g.30606881G>T GRCh38
NC_000003.11:g.30648373G>T , CM000665.1:g.30648373G>T GRCh37
NC_000003.10:g.30623377G>T NCBI36
NG_007490.1:g.5380G>T , LRG_779:g.5380G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.-3G>T MANE Select ENSP00000295754.5:n.-3G>T
ENST00000295754.9:c.-3G>T ENSP00000295754.5:n.-3G>T
ENST00000359013.4:c.-3G>T ENSP00000351905.4:n.-3G>T
NM_001024847.2:c.-3G>T , LRG_779t1:c.-3G>T NP_001020018.1:n.-3G>T
NM_003242.5:c.-3G>T NP_003233.4:n.-3G>T
XM_011534045.1:c.-12+288G>T XP_011532347.1:n.-12+288G>T
XM_011534045.3:c.-12+288G>T XP_011532347.1:n.-12+288G>T
NM_003242.6:c.-3G>T MANE Select NP_003233.4:n.-3G>T