Canonical Allele Identifier: CA413196969
Gene: BMP15 HGNC NCBI

Linked Data

gnomAD v4: X-50910785-T-A
MyVariant Identifiers: chrX:g.50653785T>A (hg19) chrX:g.50910785T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50910785T>A , CM000685.2:g.50910785T>A GRCh38
NC_000023.10:g.50653785T>A , CM000685.1:g.50653785T>A GRCh37
NC_000023.9:g.50670525T>A NCBI36
NG_012894.1:g.5002T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252677.4:c.2T>A MANE Select ENSP00000252677.3:p.Met1Lys
ENST00000252677.3:c.2T>A ENSP00000252677.3:p.Met1Lys
NM_005448.2:c.2T>A MANE Select NP_005439.2:p.Met1Lys
Search 100 bp 5'
Search 100 bp 3'