Canonical Allele Identifier: CA6588867
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs765638457
ExAC: 12:53207824 A / C
gnomAD v2: 12-53207824-A-C
gnomAD v4: 12-52814040-A-C
MyVariant Identifiers: chr12:g.53207824A>C (hg19) chr12:g.52814040A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814040A>C , CM000674.2:g.52814040A>C GRCh38
NC_000012.11:g.53207824A>C , CM000674.1:g.53207824A>C GRCh37
NC_000012.10:g.51494091A>C NCBI36
NG_007380.1:g.5512T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.19T>G MANE Select ENSP00000448220.1:p.Cys7Gly
ENST00000548097.5:c.19T>G ENSP00000449755.1:p.Cys7Gly
ENST00000551956.1:c.19T>G ENSP00000448220.1:p.Cys7Gly
ENST00000552668.1:c.19T>G ENSP00000447320.1:p.Cys7Gly
NM_002272.3:c.19T>G NP_002263.3:p.Cys7Gly
NM_002272.4:c.19T>G MANE Select NP_002263.3:p.Cys7Gly
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