Canonical Allele Identifier: CA399389051
Gene: KRT12 HGNC NCBI

Linked Data

dbSNP Id: rs1211162885
gnomAD v2: 17-39023209-A-G
gnomAD v4: 17-40866957-A-G
MyVariant Identifiers: chr17:g.39023209A>G (hg19) chr17:g.40866957A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866957A>G , CM000679.2:g.40866957A>G GRCh38
NC_000017.10:g.39023209A>G , CM000679.1:g.39023209A>G GRCh37
NC_000017.9:g.36276735A>G NCBI36
NG_008077.1:g.5254T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000251643.5:c.230T>C MANE Select ENSP00000251643.4:p.Met77Thr
ENST00000647902.1:c.211+19T>C ENSP00000497770.1:n.211+19T>C
ENST00000251643.4:c.230T>C ENSP00000251643.4:p.Met77Thr
NM_000223.3:c.230T>C NP_000214.1:p.Met77Thr
XR_934754.1:n.1500+16097A>G
XR_934754.2:n.2008+16097A>G
NM_000223.4:c.230T>C MANE Select NP_000214.1:p.Met77Thr
Search 100 bp 5'
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