Canonical Allele Identifier: CA2036598600
Gene: KRT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652077G= , CM000674.2:g.52652077G= GRCh38
NC_000012.11:g.53045861G= , CM000674.1:g.53045861G= GRCh37
NC_000012.10:g.51332128G= NCBI36
NG_008296.1:g.5099C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.66C= MANE Select ENSP00000310861.3:p.Phe22=
ENST00000309680.3:c.66C= ENSP00000310861.3:p.Phe22=
NM_000423.2:c.66C= NP_000414.2:p.Phe22=
NM_000423.3:c.66C= MANE Select NP_000414.2:p.Phe22=
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