Canonical Allele Identifier: CA516681234
Gene: BMP15 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.50658866C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50915866C>T , CM000685.2:g.50915866C>T GRCh38
NC_000023.10:g.50658866C>T , CM000685.1:g.50658866C>T GRCh37
NC_000023.9:g.50675606C>T NCBI36
NG_012894.1:g.10083C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252677.4:c.438C>T MANE Select ENSP00000252677.3:p.Phe146=
ENST00000252677.3:c.438C>T ENSP00000252677.3:p.Phe146=
NM_005448.2:c.438C>T MANE Select NP_005439.2:p.Phe146=
Search 100 bp 5'
Search 100 bp 3'