Canonical Allele Identifier: CA2036663658
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939968680
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814232C>T , CM000674.2:g.52814232C>T GRCh38
NC_000012.11:g.53208016C>T , CM000674.1:g.53208016C>T GRCh37
NC_000012.10:g.51494283C>T NCBI36
NG_007380.1:g.5320G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-174G>A ENSP00000448220.1:n.-174G>A
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