Canonical Allele Identifier: CA2036492695
Gene: KRT6C HGNC NCBI

Linked Data

dbSNP Id: rs1937836213
gnomAD v4: 12-52469612-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52469612G>A , CM000674.2:g.52469612G>A GRCh38
NC_000012.11:g.52863396G>A , CM000674.1:g.52863396G>A GRCh37
NC_000012.10:g.51149663G>A NCBI36
NG_012416.1:g.9174C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252250.7:c.1424+58C>T MANE Select ENSP00000252250.6:n.1424+58C>T
ENST00000252250.6:c.1424+58C>T ENSP00000252250.6:n.1424+58C>T
NM_173086.4:c.1424+58C>T NP_775109.2:n.1424+58C>T
NM_173086.5:c.1424+58C>T MANE Select NP_775109.2:n.1424+58C>T
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