Canonical Allele Identifier: CA413198058
Gene: BMP15 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.50658936G>T (hg19) chrX:g.50915936G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50915936G>T , CM000685.2:g.50915936G>T GRCh38
NC_000023.10:g.50658936G>T , CM000685.1:g.50658936G>T GRCh37
NC_000023.9:g.50675676G>T NCBI36
NG_012894.1:g.10153G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.508G>T MANE Select ENSP00000252677.3:p.Asp170Tyr
ENST00000252677.3:c.508G>T ENSP00000252677.3:p.Asp170Tyr
NM_005448.2:c.508G>T MANE Select NP_005439.2:p.Asp170Tyr
Search 100 bp 5'
Search 100 bp 3'