Canonical Allele Identifier: CA384954707
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1312778673
gnomAD v2: 12-52882310-A-T
MyVariant Identifiers: chr12:g.52882310A>T (hg19) chr12:g.52488526A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52488526A>T , CM000674.2:g.52488526A>T GRCh38
NC_000012.11:g.52882310A>T , CM000674.1:g.52882310A>T GRCh37
NC_000012.10:g.51168577A>T NCBI36
NG_008298.1:g.9872T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1226T>A MANE Select ENSP00000369317.3:p.Ile409Asn
ENST00000330722.6:c.1226T>A ENSP00000369317.3:p.Ile409Asn
NM_005554.3:c.1226T>A NP_005545.1:p.Ile409Asn
NM_005554.4:c.1226T>A MANE Select NP_005545.1:p.Ile409Asn
Search 100 bp 5'
Search 100 bp 3'