Canonical Allele Identifier: CA413198000
Gene: BMP15 HGNC NCBI

Linked Data

dbSNP Id: rs1923115842
MyVariant Identifiers: chrX:g.50658909A>G (hg19) chrX:g.50915909A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50915909A>G , CM000685.2:g.50915909A>G GRCh38
NC_000023.10:g.50658909A>G , CM000685.1:g.50658909A>G GRCh37
NC_000023.9:g.50675649A>G NCBI36
NG_012894.1:g.10126A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.481A>G MANE Select ENSP00000252677.3:p.Thr161Ala
ENST00000252677.3:c.481A>G ENSP00000252677.3:p.Thr161Ala
NM_005448.2:c.481A>G MANE Select NP_005439.2:p.Thr161Ala
Search 100 bp 5'
Search 100 bp 3'