Canonical Allele Identifier: CA2618946569
Gene: KRT2 HGNC NCBI

Linked Data

gnomAD v4: 12-52652148-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652148C>G , CM000674.2:g.52652148C>G GRCh38
NC_000012.11:g.53045932C>G , CM000674.1:g.53045932C>G GRCh37
NC_000012.10:g.51332199C>G NCBI36
NG_008296.1:g.5028G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.-6G>C MANE Select ENSP00000310861.3:n.-6G>C
ENST00000309680.3:c.-6G>C ENSP00000310861.3:n.-6G>C
NM_000423.2:c.-6G>C NP_000414.2:n.-6G>C
NM_000423.3:c.-6G>C MANE Select NP_000414.2:n.-6G>C
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