Canonical Allele Identifier: CA384973581
Gene: KRT75 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52827632T>G (hg19) chr12:g.52433848T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433848T>G , CM000674.2:g.52433848T>G GRCh38
NC_000012.11:g.52827632T>G , CM000674.1:g.52827632T>G GRCh37
NC_000012.10:g.51113899T>G NCBI36
NG_008403.1:g.5479A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.457A>C MANE Select ENSP00000252245.5:p.Ile153Leu
ENST00000252245.5:c.457A>C ENSP00000252245.5:p.Ile153Leu
NM_004693.2:c.457A>C NP_004684.2:p.Ile153Leu
NM_004693.3:c.457A>C MANE Select NP_004684.2:p.Ile153Leu
Search 100 bp 5'
Search 100 bp 3'