Canonical Allele Identifier: CA10416537
Gene: BMP15 HGNC NCBI

Linked Data

ClinVar Variation Id: 3049277
ClinVar RCV Id: RCV003959138 RCV004369846
dbSNP Id: rs151186104
ExAC: X:50658837 T / A
gnomAD v2: X-50658837-T-A
gnomAD v3: X-50915837-T-A
gnomAD v4: X-50915837-T-A
MyVariant Identifiers: chrX:g.50658837T>A (hg19) chrX:g.50915837T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50915837T>A , CM000685.2:g.50915837T>A GRCh38
NC_000023.10:g.50658837T>A , CM000685.1:g.50658837T>A GRCh37
NC_000023.9:g.50675577T>A NCBI36
NG_012894.1:g.10054T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.409T>A MANE Select ENSP00000252677.3:p.Tyr137Asn
ENST00000252677.3:c.409T>A ENSP00000252677.3:p.Tyr137Asn
NM_005448.2:c.409T>A MANE Select NP_005439.2:p.Tyr137Asn
Search 100 bp 5'
Search 100 bp 3'