Canonical Allele Identifier: CA384926150
Gene: KRT6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52845322C>G (hg19) chr12:g.52451538C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451538C>G , CM000674.2:g.52451538C>G GRCh38
NC_000012.11:g.52845322C>G , CM000674.1:g.52845322C>G GRCh37
NC_000012.10:g.51131589C>G NCBI36
NG_008299.1:g.5589G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.540+1G>C MANE Select ENSP00000252252.3:n.540+1G>C
ENST00000252252.3:c.540+1G>C ENSP00000252252.3:n.540+1G>C
NM_005555.3:c.540+1G>C NP_005546.2:n.540+1G>C
NM_005555.4:c.540+1G>C MANE Select NP_005546.2:n.540+1G>C
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