Canonical Allele Identifier: CA316818329
Gene: BMP7 HGNC NCBI

Linked Data

dbSNP Id: rs1022982411
MyVariant Identifiers: chr20:g.55826170G>T (hg19) chr20:g.57251114G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57251114G>T , CM000682.2:g.57251114G>T GRCh38
NC_000020.10:g.55826170G>T , CM000682.1:g.55826170G>T GRCh37
NC_000020.9:g.55259577G>T NCBI36
NG_032771.1:g.20538C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395863.8:c.418+14591C>A MANE Select ENSP00000379204.3:n.418+14591C>A
ENST00000395863.7:c.418+14591C>A ENSP00000379204.3:n.418+14591C>A
ENST00000395864.7:c.418+14591C>A ENSP00000379205.3:n.418+14591C>A
ENST00000433911.1:c.74+14591C>A
ENST00000450594.6:c.418+14591C>A ENSP00000398687.2:n.418+14591C>A
NM_001719.2:c.418+14591C>A NP_001710.1:n.418+14591C>A
NM_001719.3:c.418+14591C>A MANE Select NP_001710.1:n.418+14591C>A
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