Canonical Allele Identifier: CA6580136
Gene: KRT75 HGNC NCBI

Linked Data

dbSNP Id: rs770243826

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433812C>T , CM000674.2:g.52433812C>T GRCh38
NC_000012.11:g.52827596C>T , CM000674.1:g.52827596C>T GRCh37
NC_000012.10:g.51113863C>T NCBI36
NG_008403.1:g.5515G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.493G>A MANE Select ENSP00000252245.5:p.Asp165Asn
ENST00000252245.5:c.493G>A ENSP00000252245.5:p.Asp165Asn
NM_004693.2:c.493G>A NP_004684.2:p.Asp165Asn
NM_004693.3:c.493G>A MANE Select NP_004684.2:p.Asp165Asn