Canonical Allele Identifier: CA384954129
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1938191057
MyVariant Identifiers: chr12:g.52882229T>C (hg19) chr12:g.52488445T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488445T>C , CM000674.2:g.52488445T>C GRCh38
NC_000012.11:g.52882229T>C , CM000674.1:g.52882229T>C GRCh37
NC_000012.10:g.51168496T>C NCBI36
NG_008298.1:g.9953A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1307A>G MANE Select ENSP00000369317.3:p.Lys436Arg
ENST00000330722.6:c.1307A>G ENSP00000369317.3:p.Lys436Arg
NM_005554.3:c.1307A>G NP_005545.1:p.Lys436Arg
NM_005554.4:c.1307A>G MANE Select NP_005545.1:p.Lys436Arg
Search 100 bp 5'
Search 100 bp 3'