Canonical Allele Identifier: CA479852309
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1370912334
gnomAD v2: 12-52881651-G-A
gnomAD v3: 12-52487867-G-A
gnomAD v4: 12-52487867-G-A
MyVariant Identifiers: chr12:g.52881651G>A (hg19) chr12:g.52487867G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487867G>A , CM000674.2:g.52487867G>A GRCh38
NC_000012.11:g.52881651G>A , CM000674.1:g.52881651G>A GRCh37
NC_000012.10:g.51167918G>A NCBI36
NG_008298.1:g.10531C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330722.7:c.1548C>T MANE Select ENSP00000369317.3:p.Ser516=
ENST00000330722.6:c.1548C>T ENSP00000369317.3:p.Ser516=
NM_005554.3:c.1548C>T NP_005545.1:p.Ser516=
NM_005554.4:c.1548C>T MANE Select NP_005545.1:p.Ser516=
Search 100 bp 5'
Search 100 bp 3'