Canonical Allele Identifier: CA413197909
Gene: BMP15 HGNC NCBI

Linked Data

dbSNP Id: rs1923114442
MyVariant Identifiers: chrX:g.50658870C>T (hg19) chrX:g.50915870C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50915870C>T , CM000685.2:g.50915870C>T GRCh38
NC_000023.10:g.50658870C>T , CM000685.1:g.50658870C>T GRCh37
NC_000023.9:g.50675610C>T NCBI36
NG_012894.1:g.10087C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.442C>T MANE Select ENSP00000252677.3:p.Leu148Phe
ENST00000252677.3:c.442C>T ENSP00000252677.3:p.Leu148Phe
NM_005448.2:c.442C>T MANE Select NP_005439.2:p.Leu148Phe
Search 100 bp 5'
Search 100 bp 3'