Canonical Allele Identifier: CA2036511368
Gene: KRT75 HGNC NCBI

Linked Data

dbSNP Id: rs1940177497
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433727T>C , CM000674.2:g.52433727T>C GRCh38
NC_000012.11:g.52827511T>C , CM000674.1:g.52827511T>C GRCh37
NC_000012.10:g.51113778T>C NCBI36
NG_008403.1:g.5600A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.498+80A>G MANE Select ENSP00000252245.5:n.498+80A>G
ENST00000252245.5:c.498+80A>G ENSP00000252245.5:n.498+80A>G
NM_004693.2:c.498+80A>G NP_004684.2:n.498+80A>G
NM_004693.3:c.498+80A>G MANE Select NP_004684.2:n.498+80A>G
Search 100 bp 5'
Search 100 bp 3'