Canonical Allele Identifier: CA2618946566
Gene: KRT2 HGNC NCBI

Linked Data

gnomAD v4: 12-52652145-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652145T>C , CM000674.2:g.52652145T>C GRCh38
NC_000012.11:g.53045929T>C , CM000674.1:g.53045929T>C GRCh37
NC_000012.10:g.51332196T>C NCBI36
NG_008296.1:g.5031A>G

Transcript Alleles

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