Canonical Allele Identifier: CA479852891
Gene: KRT6A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52881735C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487951C>A , CM000674.2:g.52487951C>A GRCh38
NC_000012.11:g.52881735C>A , CM000674.1:g.52881735C>A GRCh37
NC_000012.10:g.51168002C>A NCBI36
NG_008298.1:g.10447G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1464G>T MANE Select ENSP00000369317.3:p.Val488=
ENST00000330722.6:c.1464G>T ENSP00000369317.3:p.Val488=
NM_005554.3:c.1464G>T NP_005545.1:p.Val488=
NM_005554.4:c.1464G>T MANE Select NP_005545.1:p.Val488=
Search 100 bp 5'
Search 100 bp 3'