Canonical Allele Identifier: CA6588010
Gene: KRT3 HGNC NCBI

Linked Data

dbSNP Id: rs774733153
ExAC: 12:53186074 C / T
gnomAD v2: 12-53186074-C-T
gnomAD v4: 12-52792290-C-T
COSMIC: COSM4406315
MyVariant Identifiers: chr12:g.53186074C>T (hg19) chr12:g.52792290C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52792290C>T , CM000674.2:g.52792290C>T GRCh38
NC_000012.11:g.53186074C>T , CM000674.1:g.53186074C>T GRCh37
NC_000012.10:g.51472341C>T NCBI36
NG_008350.1:g.8819G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000417996.2:c.1137G>A MANE Select ENSP00000413479.2:p.Glu379=
NM_057088.2:c.1137G>A NP_476429.2:p.Glu379=
XM_011538324.1:c.777G>A XP_011536626.1:p.Glu259=
XM_024448975.1:c.1401G>A XP_024304743.1:p.Glu467=
NM_057088.3:c.1137G>A MANE Select NP_476429.2:p.Glu379=
Search 100 bp 5'
Search 100 bp 3'