Canonical Allele Identifier: CA2036663722
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939970994
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814388G>A , CM000674.2:g.52814388G>A GRCh38
NC_000012.11:g.53208172G>A , CM000674.1:g.53208172G>A GRCh37
NC_000012.10:g.51494439G>A NCBI36
NG_007380.1:g.5164C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-330C>T ENSP00000448220.1:n.-330C>T
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