Canonical Allele Identifier: CA480068929
Gene: KRT6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52841651C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52447867C>G , CM000674.2:g.52447867C>G GRCh38
NC_000012.11:g.52841651C>G , CM000674.1:g.52841651C>G GRCh37
NC_000012.10:g.51127918C>G NCBI36
NG_008299.1:g.9260G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.1335G>C MANE Select ENSP00000252252.3:p.Leu445=
ENST00000252252.3:c.1335G>C ENSP00000252252.3:p.Leu445=
NM_005555.3:c.1335G>C NP_005546.2:p.Leu445=
NM_005555.4:c.1335G>C MANE Select NP_005546.2:p.Leu445=
Search 100 bp 5'
Search 100 bp 3'