Canonical Allele Identifier: CA384973516
Gene: KRT75 HGNC NCBI

Linked Data

gnomAD v4: 12-52433836-T-C
MyVariant Identifiers: chr12:g.52827620T>C (hg19) chr12:g.52433836T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433836T>C , CM000674.2:g.52433836T>C GRCh38
NC_000012.11:g.52827620T>C , CM000674.1:g.52827620T>C GRCh37
NC_000012.10:g.51113887T>C NCBI36
NG_008403.1:g.5491A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.469A>G MANE Select ENSP00000252245.5:p.Asn157Asp
ENST00000252245.5:c.469A>G ENSP00000252245.5:p.Asn157Asp
NM_004693.2:c.469A>G NP_004684.2:p.Asn157Asp
NM_004693.3:c.469A>G MANE Select NP_004684.2:p.Asn157Asp
Search 100 bp 5'
Search 100 bp 3'