Canonical Allele Identifier: CA10416476
Gene: BMP15 HGNC NCBI

Linked Data

dbSNP Id: rs782634938
ExAC: X:50653816 T / C
gnomAD v2: X-50653816-T-C
gnomAD v4: X-50910816-T-C
MyVariant Identifiers: chrX:g.50653816T>C (hg19) chrX:g.50910816T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50910816T>C , CM000685.2:g.50910816T>C GRCh38
NC_000023.10:g.50653816T>C , CM000685.1:g.50653816T>C GRCh37
NC_000023.9:g.50670556T>C NCBI36
NG_012894.1:g.5033T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.33T>C MANE Select ENSP00000252677.3:p.Phe11=
ENST00000252677.3:c.33T>C ENSP00000252677.3:p.Phe11=
NM_005448.2:c.33T>C MANE Select NP_005439.2:p.Phe11=
Search 100 bp 5'
Search 100 bp 3'