Canonical Allele Identifier: CA181687813
Gene: CALB1 HGNC NCBI

Linked Data

dbSNP Id: rs979904309
MyVariant Identifiers: chr8:g.91095429T>A (hg19) chr8:g.90083201T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.90083201T>A , CM000670.2:g.90083201T>A GRCh38
NC_000008.10:g.91095429T>A , CM000670.1:g.91095429T>A GRCh37
NC_000008.9:g.91164605T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000514406.2:c.-92-1099A>T ENSP00000430192.1:n.-92-1099A>T
ENST00000520613.5:c.-92-1099A>T ENSP00000430281.1:n.-92-1099A>T
ENST00000523716.5:c.-92-1099A>T ENSP00000429246.1:n.-92-1099A>T
Search 100 bp 5'
Search 100 bp 3'