Canonical Allele Identifier: CA479852308
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1938174946
MyVariant Identifiers: chr12:g.52881645G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487861G>T , CM000674.2:g.52487861G>T GRCh38
NC_000012.11:g.52881645G>T , CM000674.1:g.52881645G>T GRCh37
NC_000012.10:g.51167912G>T NCBI36
NG_008298.1:g.10537C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1554C>A MANE Select ENSP00000369317.3:p.Gly518=
ENST00000330722.6:c.1554C>A ENSP00000369317.3:p.Gly518=
NM_005554.3:c.1554C>A NP_005545.1:p.Gly518=
NM_005554.4:c.1554C>A MANE Select NP_005545.1:p.Gly518=
Search 100 bp 5'
Search 100 bp 3'