Canonical Allele Identifier: CA2618933008
Gene: KRT5 HGNC NCBI

Linked Data

gnomAD v4: 12-52520398-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520398C>A , CM000674.2:g.52520398C>A GRCh38
NC_000012.11:g.52914182C>A , CM000674.1:g.52914182C>A GRCh37
NC_000012.10:g.51200449C>A NCBI36
NG_008297.1:g.5062G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.8:c.-102G>T ENSP00000252242.4:n.-102G>T
ENST00000546577.1:c.-14G>T ENSP00000449651.1:n.-14G>T
NM_000424.3:c.-102G>T NP_000415.2:n.-102G>T
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