Canonical Allele Identifier: CA605088165
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1198098228
gnomAD v2: 12-53208165-C-T
gnomAD v3: 12-52814381-C-T
gnomAD v4: 12-52814381-C-T
MyVariant Identifiers: chr12:g.53208165C>T (hg19) chr12:g.52814381C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814381C>T , CM000674.2:g.52814381C>T GRCh38
NC_000012.11:g.53208165C>T , CM000674.1:g.53208165C>T GRCh37
NC_000012.10:g.51494432C>T NCBI36
NG_007380.1:g.5171G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-323G>A ENSP00000448220.1:n.-323G>A
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