Canonical Allele Identifier: CA499971816
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023418G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867166G>C , CM000679.2:g.40867166G>C GRCh38
NC_000017.10:g.39023418G>C , CM000679.1:g.39023418G>C GRCh37
NC_000017.9:g.36276944G>C NCBI36
NG_008077.1:g.5045C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.21C>G MANE Select ENSP00000251643.4:p.Thr7=
ENST00000647902.1:c.21C>G ENSP00000497770.1:p.Thr7=
ENST00000251643.4:c.21C>G ENSP00000251643.4:p.Thr7=
NM_000223.3:c.21C>G NP_000214.1:p.Thr7=
XR_934754.1:n.1500+16306G>C
XR_934754.2:n.2008+16306G>C
NM_000223.4:c.21C>G MANE Select NP_000214.1:p.Thr7=
Search 100 bp 5'
Search 100 bp 3'