Canonical Allele Identifier: CA509817751
Gene: BMP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.6750944G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.6770297G>T , CM000682.2:g.6770297G>T GRCh38
NC_000020.10:g.6750944G>T , CM000682.1:g.6750944G>T GRCh37
NC_000020.9:g.6698944G>T NCBI36
NG_023233.1:g.7200G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378827.5:c.171G>T MANE Select ENSP00000368104.3:p.Leu57=
ENST00000378827.4:c.171G>T ENSP00000368104.3:p.Leu57=
NM_001200.2:c.171G>T NP_001191.1:p.Leu57=
XM_011529323.1:c.-123+1422G>T XP_011527625.1:n.-123+1422G>T
NM_001200.3:c.171G>T NP_001191.1:p.Leu57=
NM_001200.4:c.171G>T MANE Select NP_001191.1:p.Leu57=