Canonical Allele Identifier: CA2618946572
Gene: KRT2 HGNC NCBI

Linked Data

gnomAD v4: 12-52652152-GT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652153del , CM000674.2:g.52652153del GRCh38
NC_000012.11:g.53045937del , CM000674.1:g.53045937del GRCh37
NC_000012.10:g.51332204del NCBI36
NG_008296.1:g.5023del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.-11del MANE Select ENSP00000310861.3:n.-11del
ENST00000309680.3:c.-11del ENSP00000310861.3:n.-11del
NM_000423.2:c.-11del NP_000414.2:n.-11del
NM_000423.3:c.-11del MANE Select NP_000414.2:n.-11del
Search 100 bp 5'
Search 100 bp 3'