Canonical Allele Identifier: CA480068189
Gene: KRT6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52845455T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451671T>C , CM000674.2:g.52451671T>C GRCh38
NC_000012.11:g.52845455T>C , CM000674.1:g.52845455T>C GRCh37
NC_000012.10:g.51131722T>C NCBI36
NG_008299.1:g.5456A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.408A>G MANE Select ENSP00000252252.3:p.Gln136=
ENST00000252252.3:c.408A>G ENSP00000252252.3:p.Gln136=
NM_005555.3:c.408A>G NP_005546.2:p.Gln136=
NM_005555.4:c.408A>G MANE Select NP_005546.2:p.Gln136=
Search 100 bp 5'
Search 100 bp 3'