Canonical Allele Identifier: CA384973699
Gene: KRT75 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52827655A>C (hg19) chr12:g.52433871A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433871A>C , CM000674.2:g.52433871A>C GRCh38
NC_000012.11:g.52827655A>C , CM000674.1:g.52827655A>C GRCh37
NC_000012.10:g.51113922A>C NCBI36
NG_008403.1:g.5456T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.434T>G MANE Select ENSP00000252245.5:p.Val145Gly
ENST00000252245.5:c.434T>G ENSP00000252245.5:p.Val145Gly
NM_004693.2:c.434T>G NP_004684.2:p.Val145Gly
NM_004693.3:c.434T>G MANE Select NP_004684.2:p.Val145Gly
Search 100 bp 5'
Search 100 bp 3'