Canonical Allele Identifier: CA516681099
Gene: BMP15 HGNC NCBI

Linked Data

gnomAD v4: X-50916121-C-T
MyVariant Identifiers: chrX:g.50659121C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50916121C>T , CM000685.2:g.50916121C>T GRCh38
NC_000023.10:g.50659121C>T , CM000685.1:g.50659121C>T GRCh37
NC_000023.9:g.50675861C>T NCBI36
NG_012894.1:g.10338C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.693C>T MANE Select ENSP00000252677.3:p.Phe231=
ENST00000252677.3:c.693C>T ENSP00000252677.3:p.Phe231=
NM_005448.2:c.693C>T MANE Select NP_005439.2:p.Phe231=
Search 100 bp 5'
Search 100 bp 3'