Canonical Allele Identifier: CA237279152
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs757389220
MyVariant Identifiers: chr12:g.53208125C>A (hg19) chr12:g.52814341C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814341C>A , CM000674.2:g.52814341C>A GRCh38
NC_000012.11:g.53208125C>A , CM000674.1:g.53208125C>A GRCh37
NC_000012.10:g.51494392C>A NCBI36
NG_007380.1:g.5211G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-283G>T ENSP00000448220.1:n.-283G>T
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