Canonical Allele Identifier: CA2581088259
Gene: KRT5 HGNC NCBI

Linked Data

gnomAD v4: 12-52520427-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520427T>G , CM000674.2:g.52520427T>G GRCh38
NC_000012.11:g.52914211T>G , CM000674.1:g.52914211T>G GRCh37
NC_000012.10:g.51200478T>G NCBI36
NG_008297.1:g.5033A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.8:c.-131A>C ENSP00000252242.4:n.-131A>C
ENST00000546577.1:c.-43A>C ENSP00000449651.1:n.-43A>C
NM_000424.3:c.-131A>C NP_000415.2:n.-131A>C
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