Canonical Allele Identifier: CA384946736
Gene: KRT2 HGNC NCBI

Linked Data

gnomAD v4: 12-52652141-A-T
MyVariant Identifiers: chr12:g.53045925A>T (hg19) chr12:g.52652141A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652141A>T , CM000674.2:g.52652141A>T GRCh38
NC_000012.11:g.53045925A>T , CM000674.1:g.53045925A>T GRCh37
NC_000012.10:g.51332192A>T NCBI36
NG_008296.1:g.5035T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.2T>A MANE Select ENSP00000310861.3:p.Met1Lys
ENST00000309680.3:c.2T>A ENSP00000310861.3:p.Met1Lys
NM_000423.2:c.2T>A NP_000414.2:p.Met1Lys
NM_000423.3:c.2T>A MANE Select NP_000414.2:p.Met1Lys
Search 100 bp 5'
Search 100 bp 3'