Canonical Allele Identifier: CA500187311
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023211G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866959G>C , CM000679.2:g.40866959G>C GRCh38
NC_000017.10:g.39023211G>C , CM000679.1:g.39023211G>C GRCh37
NC_000017.9:g.36276737G>C NCBI36
NG_008077.1:g.5252C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251643.5:c.228C>G MANE Select ENSP00000251643.4:p.Ser76=
ENST00000647902.1:c.211+17C>G ENSP00000497770.1:n.211+17C>G
ENST00000251643.4:c.228C>G ENSP00000251643.4:p.Ser76=
NM_000223.3:c.228C>G NP_000214.1:p.Ser76=
XR_934754.1:n.1500+16099G>C
XR_934754.2:n.2008+16099G>C
NM_000223.4:c.228C>G MANE Select NP_000214.1:p.Ser76=
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