Canonical Allele Identifier: CA384927488
Gene: KRT6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52845456T>A (hg19) chr12:g.52451672T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451672T>A , CM000674.2:g.52451672T>A GRCh38
NC_000012.11:g.52845456T>A , CM000674.1:g.52845456T>A GRCh37
NC_000012.10:g.51131723T>A NCBI36
NG_008299.1:g.5455A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.407A>T MANE Select ENSP00000252252.3:p.Gln136Leu
ENST00000252252.3:c.407A>T ENSP00000252252.3:p.Gln136Leu
NM_005555.3:c.407A>T NP_005546.2:p.Gln136Leu
NM_005555.4:c.407A>T MANE Select NP_005546.2:p.Gln136Leu
Search 100 bp 5'
Search 100 bp 3'