Canonical Allele Identifier: CA384982029
Gene: KRT6B HGNC NCBI

Linked Data

gnomAD v4: 12-52447844-T-A
MyVariant Identifiers: chr12:g.52841628T>A (hg19) chr12:g.52447844T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447844T>A , CM000674.2:g.52447844T>A GRCh38
NC_000012.11:g.52841628T>A , CM000674.1:g.52841628T>A GRCh37
NC_000012.10:g.51127895T>A NCBI36
NG_008299.1:g.9283A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.1358A>T MANE Select ENSP00000252252.3:p.Asn453Ile
ENST00000252252.3:c.1358A>T ENSP00000252252.3:p.Asn453Ile
NM_005555.3:c.1358A>T NP_005546.2:p.Asn453Ile
NM_005555.4:c.1358A>T MANE Select NP_005546.2:p.Asn453Ile
Search 100 bp 5'
Search 100 bp 3'