Canonical Allele Identifier: CA2036598681
Gene: KRT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652163A= , CM000674.2:g.52652163A= GRCh38
NC_000012.11:g.53045947A= , CM000674.1:g.53045947A= GRCh37
NC_000012.10:g.51332214A= NCBI36
NG_008296.1:g.5013T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.-21T= MANE Select ENSP00000310861.3:n.-21T=
ENST00000309680.3:c.-21T= ENSP00000310861.3:n.-21T=
NM_000423.2:c.-21T= NP_000414.2:n.-21T=
NM_000423.3:c.-21T= MANE Select NP_000414.2:n.-21T=
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