Canonical Allele Identifier: CA6588926
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs779356218
ExAC: 12:53208081 A / C
gnomAD v2: 12-53208081-A-C
gnomAD v4: 12-52814297-A-C
MyVariant Identifiers: chr12:g.53208081A>C (hg19) chr12:g.52814297A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814297A>C , CM000674.2:g.52814297A>C GRCh38
NC_000012.11:g.53208081A>C , CM000674.1:g.53208081A>C GRCh37
NC_000012.10:g.51494348A>C NCBI36
NG_007380.1:g.5255T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-239T>G ENSP00000448220.1:n.-239T>G
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