Canonical Allele Identifier: CA480067620
Gene: KRT75 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52827651C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433867C>G , CM000674.2:g.52433867C>G GRCh38
NC_000012.11:g.52827651C>G , CM000674.1:g.52827651C>G GRCh37
NC_000012.10:g.51113918C>G NCBI36
NG_008403.1:g.5460G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.438G>C MANE Select ENSP00000252245.5:p.Arg146=
ENST00000252245.5:c.438G>C ENSP00000252245.5:p.Arg146=
NM_004693.2:c.438G>C NP_004684.2:p.Arg146=
NM_004693.3:c.438G>C MANE Select NP_004684.2:p.Arg146=
Search 100 bp 5'
Search 100 bp 3'