Canonical Allele Identifier: CA516681119
Gene: BMP15 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.50659130C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50916130C>A , CM000685.2:g.50916130C>A GRCh38
NC_000023.10:g.50659130C>A , CM000685.1:g.50659130C>A GRCh37
NC_000023.9:g.50675870C>A NCBI36
NG_012894.1:g.10347C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.702C>A MANE Select ENSP00000252677.3:p.Leu234=
ENST00000252677.3:c.702C>A ENSP00000252677.3:p.Leu234=
NM_005448.2:c.702C>A MANE Select NP_005439.2:p.Leu234=