Canonical Allele Identifier: CA357620330
Gene: IBSP HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88732513G>T (hg19) chr4:g.87811361G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811361G>T , CM000666.2:g.87811361G>T GRCh38
NC_000004.11:g.88732513G>T , CM000666.1:g.88732513G>T GRCh37
NC_000004.10:g.88951537G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000226284.7:c.406-1G>T MANE Select ENSP00000226284.5:n.406-1G>T
ENST00000226284.6:c.406-1G>T ENSP00000226284.5:n.406-1G>T
NM_004967.3:c.406-1G>T NP_004958.2:n.406-1G>T
NM_004967.4:c.406-1G>T MANE Select NP_004958.2:n.406-1G>T
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Search 100 bp 3'