Canonical Allele Identifier: CA480069822
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1338685696
gnomAD v2: 12-52886463-G-A
gnomAD v4: 12-52492679-G-A
MyVariant Identifiers: chr12:g.52886463G>A (hg19) chr12:g.52492679G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492679G>A , CM000674.2:g.52492679G>A GRCh38
NC_000012.11:g.52886463G>A , CM000674.1:g.52886463G>A GRCh37
NC_000012.10:g.51172730G>A NCBI36
NG_008298.1:g.5719C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.510C>T MANE Select ENSP00000369317.3:p.Leu170=
ENST00000330722.6:c.510C>T ENSP00000369317.3:p.Leu170=
ENST00000549898.5:n.31C>T
NM_005554.3:c.510C>T NP_005545.1:p.Leu170=
NM_005554.4:c.510C>T MANE Select NP_005545.1:p.Leu170=
Search 100 bp 5'
Search 100 bp 3'