Canonical Allele Identifier: CA384952899
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1486207188

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487923C>T , CM000674.2:g.52487923C>T GRCh38
NC_000012.11:g.52881707C>T , CM000674.1:g.52881707C>T GRCh37
NC_000012.10:g.51167974C>T NCBI36
NG_008298.1:g.10475G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1492G>A MANE Select ENSP00000369317.3:p.Gly498Ser
ENST00000330722.6:c.1492G>A ENSP00000369317.3:p.Gly498Ser
NM_005554.3:c.1492G>A NP_005545.1:p.Gly498Ser
NM_005554.4:c.1492G>A MANE Select NP_005545.1:p.Gly498Ser