Canonical Allele Identifier: CA516681242
Gene: BMP15 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.50658869T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50915869T>C , CM000685.2:g.50915869T>C GRCh38
NC_000023.10:g.50658869T>C , CM000685.1:g.50658869T>C GRCh37
NC_000023.9:g.50675609T>C NCBI36
NG_012894.1:g.10086T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.441T>C MANE Select ENSP00000252677.3:p.Asn147=
ENST00000252677.3:c.441T>C ENSP00000252677.3:p.Asn147=
NM_005448.2:c.441T>C MANE Select NP_005439.2:p.Asn147=