Canonical Allele Identifier: CA516681298
Gene: BMP15 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.50658926C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50915926C>G , CM000685.2:g.50915926C>G GRCh38
NC_000023.10:g.50658926C>G , CM000685.1:g.50658926C>G GRCh37
NC_000023.9:g.50675666C>G NCBI36
NG_012894.1:g.10143C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.498C>G MANE Select ENSP00000252677.3:p.Ser166=
ENST00000252677.3:c.498C>G ENSP00000252677.3:p.Ser166=
NM_005448.2:c.498C>G MANE Select NP_005439.2:p.Ser166=
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