Canonical Allele Identifier: CA876101733
Gene: BMP15 HGNC NCBI

Linked Data

dbSNP Id: rs1159458671
MyVariant Identifiers: chrX:g.50911141G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50911141G>T , CM000685.2:g.50911141G>T GRCh38
NC_000023.10:g.50654141G>T , CM000685.1:g.50654141G>T GRCh37
NC_000023.9:g.50670881G>T NCBI36
NG_012894.1:g.5358G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.328+30G>T MANE Select ENSP00000252677.3:n.328+30G>T
ENST00000252677.3:c.328+30G>T ENSP00000252677.3:n.328+30G>T
NM_005448.2:c.328+30G>T MANE Select NP_005439.2:n.328+30G>T