Canonical Allele Identifier: CA625984978
Gene: KRT12 HGNC NCBI

Linked Data

dbSNP Id: rs1192037520
gnomAD v2: 17-39023457-A-G
gnomAD v3: 17-40867205-A-G
gnomAD v4: 17-40867205-A-G
MyVariant Identifiers: chr17:g.39023457A>G (hg19) chr17:g.40867205A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867205A>G , CM000679.2:g.40867205A>G GRCh38
NC_000017.10:g.39023457A>G , CM000679.1:g.39023457A>G GRCh37
NC_000017.9:g.36276983A>G NCBI36
NG_008077.1:g.5006T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.-19T>C MANE Select ENSP00000251643.4:n.-19T>C
ENST00000251643.4:c.-19T>C ENSP00000251643.4:n.-19T>C
NM_000223.3:c.-19T>C NP_000214.1:n.-19T>C
XR_934754.1:n.1500+16345A>G
XR_934754.2:n.2008+16345A>G
NM_000223.4:c.-19T>C MANE Select NP_000214.1:n.-19T>C
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