Canonical Allele Identifier: CA413198026
Gene: BMP15 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.50658920C>A (hg19) chrX:g.50915920C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50915920C>A , CM000685.2:g.50915920C>A GRCh38
NC_000023.10:g.50658920C>A , CM000685.1:g.50658920C>A GRCh37
NC_000023.9:g.50675660C>A NCBI36
NG_012894.1:g.10137C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.492C>A MANE Select ENSP00000252677.3:p.Phe164Leu
ENST00000252677.3:c.492C>A ENSP00000252677.3:p.Phe164Leu
NM_005448.2:c.492C>A MANE Select NP_005439.2:p.Phe164Leu
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