Canonical Allele Identifier: CA329809488
Gene: BMP15 HGNC NCBI

Linked Data

dbSNP Id: rs905130335
gnomAD v4: X-50911170-G-C
MyVariant Identifiers: chrX:g.50911170G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.50911170G>C , CM000685.2:g.50911170G>C GRCh38
NC_000023.10:g.50654170G>C , CM000685.1:g.50654170G>C GRCh37
NC_000023.9:g.50670910G>C NCBI36
NG_012894.1:g.5387G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252677.4:c.328+59G>C MANE Select ENSP00000252677.3:n.328+59G>C
ENST00000252677.3:c.328+59G>C ENSP00000252677.3:n.328+59G>C
NM_005448.2:c.328+59G>C MANE Select NP_005439.2:n.328+59G>C
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