Canonical Allele Identifier: CA413198047
Gene: BMP15 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.50658930G>C (hg19) chrX:g.50915930G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50915930G>C , CM000685.2:g.50915930G>C GRCh38
NC_000023.10:g.50658930G>C , CM000685.1:g.50658930G>C GRCh37
NC_000023.9:g.50675670G>C NCBI36
NG_012894.1:g.10147G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.502G>C MANE Select ENSP00000252677.3:p.Glu168Gln
ENST00000252677.3:c.502G>C ENSP00000252677.3:p.Glu168Gln
NM_005448.2:c.502G>C MANE Select NP_005439.2:p.Glu168Gln
Search 100 bp 5'
Search 100 bp 3'