Canonical Allele Identifier: CA516681199
Gene: BMP15 HGNC NCBI

Linked Data

dbSNP Id: rs2147792000
MyVariant Identifiers: chrX:g.50654083C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50911083C>T , CM000685.2:g.50911083C>T GRCh38
NC_000023.10:g.50654083C>T , CM000685.1:g.50654083C>T GRCh37
NC_000023.9:g.50670823C>T NCBI36
NG_012894.1:g.5300C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.300C>T MANE Select ENSP00000252677.3:p.Pro100=
ENST00000252677.3:c.300C>T ENSP00000252677.3:p.Pro100=
NM_005448.2:c.300C>T MANE Select NP_005439.2:p.Pro100=