Canonical Allele Identifier: CA384953007
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1405909933
MyVariant Identifiers: chr12:g.52881727G>C (hg19) chr12:g.52487943G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487943G>C , CM000674.2:g.52487943G>C GRCh38
NC_000012.11:g.52881727G>C , CM000674.1:g.52881727G>C GRCh37
NC_000012.10:g.51167994G>C NCBI36
NG_008298.1:g.10455C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1472C>G MANE Select ENSP00000369317.3:p.Ser491Cys
ENST00000330722.6:c.1472C>G ENSP00000369317.3:p.Ser491Cys
NM_005554.3:c.1472C>G NP_005545.1:p.Ser491Cys
NM_005554.4:c.1472C>G MANE Select NP_005545.1:p.Ser491Cys
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Search 100 bp 3'