Canonical Allele Identifier: CA516681000
Gene: BMP15 HGNC NCBI

Linked Data

dbSNP Id: rs1923002707
gnomAD v4: X-50910994-C-T
MyVariant Identifiers: chrX:g.50653994C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50910994C>T , CM000685.2:g.50910994C>T GRCh38
NC_000023.10:g.50653994C>T , CM000685.1:g.50653994C>T GRCh37
NC_000023.9:g.50670734C>T NCBI36
NG_012894.1:g.5211C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.211C>T MANE Select ENSP00000252677.3:p.Leu71=
ENST00000252677.3:c.211C>T ENSP00000252677.3:p.Leu71=
NM_005448.2:c.211C>T MANE Select NP_005439.2:p.Leu71=
Search 100 bp 5'
Search 100 bp 3'