Canonical Allele Identifier: CA413198486
Gene: BMP15 HGNC NCBI

Linked Data

gnomAD v4: X-50916129-T-A
MyVariant Identifiers: chrX:g.50659129T>A (hg19) chrX:g.50916129T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50916129T>A , CM000685.2:g.50916129T>A GRCh38
NC_000023.10:g.50659129T>A , CM000685.1:g.50659129T>A GRCh37
NC_000023.9:g.50675869T>A NCBI36
NG_012894.1:g.10346T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.701T>A MANE Select ENSP00000252677.3:p.Leu234His
ENST00000252677.3:c.701T>A ENSP00000252677.3:p.Leu234His
NM_005448.2:c.701T>A MANE Select NP_005439.2:p.Leu234His
Search 100 bp 5'
Search 100 bp 3'