Canonical Allele Identifier: CA384973407
Gene: KRT75 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52827602A>C (hg19) chr12:g.52433818A>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.487T>G MANE Select ENSP00000252245.5:p.Phe163Val
ENST00000252245.5:c.487T>G ENSP00000252245.5:p.Phe163Val
NM_004693.2:c.487T>G NP_004684.2:p.Phe163Val
NM_004693.3:c.487T>G MANE Select NP_004684.2:p.Phe163Val
Search 100 bp 5'
Search 100 bp 3'