Canonical Allele Identifier: CA500187392
Gene: KRT12 HGNC NCBI

Linked Data

dbSNP Id: rs1907055808
gnomAD v3: 17-40867010-A-C
gnomAD v4: 17-40867010-A-C
MyVariant Identifiers: chr17:g.39023262A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867010A>C , CM000679.2:g.40867010A>C GRCh38
NC_000017.10:g.39023262A>C , CM000679.1:g.39023262A>C GRCh37
NC_000017.9:g.36276788A>C NCBI36
NG_008077.1:g.5201T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.177T>G MANE Select ENSP00000251643.4:p.Ala59=
ENST00000647902.1:c.177T>G ENSP00000497770.1:p.Ala59=
ENST00000251643.4:c.177T>G ENSP00000251643.4:p.Ala59=
NM_000223.3:c.177T>G NP_000214.1:p.Ala59=
XR_934754.1:n.1500+16150A>C
XR_934754.2:n.2008+16150A>C
NM_000223.4:c.177T>G MANE Select NP_000214.1:p.Ala59=
Search 100 bp 5'
Search 100 bp 3'