Canonical Allele Identifier: CA384973409
Gene: KRT75 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52827602A>G (hg19) chr12:g.52433818A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433818A>G , CM000674.2:g.52433818A>G GRCh38
NC_000012.11:g.52827602A>G , CM000674.1:g.52827602A>G GRCh37
NC_000012.10:g.51113869A>G NCBI36
NG_008403.1:g.5509T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.487T>C MANE Select ENSP00000252245.5:p.Phe163Leu
ENST00000252245.5:c.487T>C ENSP00000252245.5:p.Phe163Leu
NM_004693.2:c.487T>C NP_004684.2:p.Phe163Leu
NM_004693.3:c.487T>C MANE Select NP_004684.2:p.Phe163Leu
Search 100 bp 5'
Search 100 bp 3'