Canonical Allele Identifier: CA357620662
Gene: IBSP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811450G>T , CM000666.2:g.87811450G>T GRCh38
NC_000004.11:g.88732602G>T , CM000666.1:g.88732602G>T GRCh37
NC_000004.10:g.88951626G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000226284.7:c.494G>T MANE Select ENSP00000226284.5:p.Ser165Ile
ENST00000226284.6:c.494G>T ENSP00000226284.5:p.Ser165Ile
NM_004967.3:c.494G>T NP_004958.2:p.Ser165Ile
NM_004967.4:c.494G>T MANE Select NP_004958.2:p.Ser165Ile