Canonical Allele Identifier: CA289714
Gene: BMP15 HGNC NCBI

Linked Data

ClinVar Variation Id: 136522
dbSNP Id: rs3810682
gnomAD v2: X-50653775-C-G
gnomAD v3: X-50910775-C-G
gnomAD v4: X-50910775-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50910775C>G , CM000685.2:g.50910775C>G GRCh38
NC_000023.10:g.50653775C>G , CM000685.1:g.50653775C>G GRCh37
NC_000023.9:g.50670515C>G NCBI36
NG_012894.1:g.4992C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252677.4:c.-9C>G MANE Select ENSP00000252677.3:n.-9C>G
NM_005448.2:c.-9C>G MANE Select NP_005439.2:n.-9C>G