Canonical Allele Identifier: CA433009885
Gene: TGFBR2 HGNC NCBI

Linked Data

gnomAD v4: 3-30606895-G-C
MyVariant Identifiers: chr3:g.30648387G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606895G>C , CM000665.2:g.30606895G>C GRCh38
NC_000003.11:g.30648387G>C , CM000665.1:g.30648387G>C GRCh37
NC_000003.10:g.30623391G>C NCBI36
NG_007490.1:g.5394G>C , LRG_779:g.5394G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.12G>C MANE Select ENSP00000295754.5:p.Gly4=
ENST00000295754.9:c.12G>C ENSP00000295754.5:p.Gly4=
ENST00000359013.4:c.12G>C ENSP00000351905.4:p.Gly4=
NM_001024847.2:c.12G>C , LRG_779t1:c.12G>C NP_001020018.1:p.Gly4=
NM_003242.5:c.12G>C NP_003233.4:p.Gly4=
XM_011534045.1:c.-12+302G>C XP_011532347.1:n.-12+302G>C
XM_011534045.3:c.-12+302G>C XP_011532347.1:n.-12+302G>C
NM_003242.6:c.12G>C MANE Select NP_003233.4:p.Gly4=
Search 100 bp 5'
Search 100 bp 3'