Canonical Allele Identifier: CA2036500180
Gene: KRT6B HGNC NCBI

Linked Data

dbSNP Id: rs1940398573
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451305G>C , CM000674.2:g.52451305G>C GRCh38
NC_000012.11:g.52845089G>C , CM000674.1:g.52845089G>C GRCh37
NC_000012.10:g.51131356G>C NCBI36
NG_008299.1:g.5822C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.540+234C>G MANE Select ENSP00000252252.3:n.540+234C>G
ENST00000252252.3:c.540+234C>G ENSP00000252252.3:n.540+234C>G
NM_005555.3:c.540+234C>G NP_005546.2:n.540+234C>G
NM_005555.4:c.540+234C>G MANE Select NP_005546.2:n.540+234C>G
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