Canonical Allele Identifier: CA2580587310
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30608572A>C , CM000665.2:g.30608572A>C GRCh38
NC_000003.11:g.30650064A>C , CM000665.1:g.30650064A>C GRCh37
NC_000003.10:g.30625068A>C NCBI36
NG_007490.1:g.7071A>C , LRG_779:g.7071A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.94+1595A>C MANE Select ENSP00000295754.5:n.94+1595A>C
ENST00000295754.9:c.94+1595A>C ENSP00000295754.5:n.94+1595A>C
ENST00000359013.4:c.94+1595A>C ENSP00000351905.4:n.94+1595A>C
NM_001024847.2:c.94+1595A>C , LRG_779t1:c.94+1595A>C NP_001020018.1:n.94+1595A>C
NM_003242.5:c.94+1595A>C NP_003233.4:n.94+1595A>C
XM_011534045.1:c.-12+1979A>C XP_011532347.1:n.-12+1979A>C
XM_011534045.3:c.-12+1979A>C XP_011532347.1:n.-12+1979A>C
NM_003242.6:c.94+1595A>C MANE Select NP_003233.4:n.94+1595A>C