Canonical Allele Identifier: CA876101742
Gene: BMP15 HGNC NCBI

Linked Data

dbSNP Id: rs1420484186
gnomAD v3: X-50911168-G-C
gnomAD v4: X-50911168-G-C
MyVariant Identifiers: chrX:g.50911168G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50911168G>C , CM000685.2:g.50911168G>C GRCh38
NC_000023.10:g.50654168G>C , CM000685.1:g.50654168G>C GRCh37
NC_000023.9:g.50670908G>C NCBI36
NG_012894.1:g.5385G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.328+57G>C MANE Select ENSP00000252677.3:n.328+57G>C
ENST00000252677.3:c.328+57G>C ENSP00000252677.3:n.328+57G>C
NM_005448.2:c.328+57G>C MANE Select NP_005439.2:n.328+57G>C