Canonical Allele Identifier: CA516681134
Gene: BMP15 HGNC NCBI

Linked Data

gnomAD v4: X-50911056-G-T
MyVariant Identifiers: chrX:g.50654056G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50911056G>T , CM000685.2:g.50911056G>T GRCh38
NC_000023.10:g.50654056G>T , CM000685.1:g.50654056G>T GRCh37
NC_000023.9:g.50670796G>T NCBI36
NG_012894.1:g.5273G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.273G>T MANE Select ENSP00000252677.3:p.Gly91=
ENST00000252677.3:c.273G>T ENSP00000252677.3:p.Gly91=
NM_005448.2:c.273G>T MANE Select NP_005439.2:p.Gly91=
Search 100 bp 5'
Search 100 bp 3'