Canonical Allele Identifier: CA516681285
Gene: BMP15 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.50658911C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50915911C>A , CM000685.2:g.50915911C>A GRCh38
NC_000023.10:g.50658911C>A , CM000685.1:g.50658911C>A GRCh37
NC_000023.9:g.50675651C>A NCBI36
NG_012894.1:g.10128C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.483C>A MANE Select ENSP00000252677.3:p.Thr161=
ENST00000252677.3:c.483C>A ENSP00000252677.3:p.Thr161=
NM_005448.2:c.483C>A MANE Select NP_005439.2:p.Thr161=
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