Canonical Allele Identifier: CA500187563
Gene: KRT12 HGNC NCBI

Linked Data

gnomAD v4: 17-40867085-A-C
MyVariant Identifiers: chr17:g.39023337A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867085A>C , CM000679.2:g.40867085A>C GRCh38
NC_000017.10:g.39023337A>C , CM000679.1:g.39023337A>C GRCh37
NC_000017.9:g.36276863A>C NCBI36
NG_008077.1:g.5126T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.102T>G MANE Select ENSP00000251643.4:p.Ser34=
ENST00000647902.1:c.102T>G ENSP00000497770.1:p.Ser34=
ENST00000251643.4:c.102T>G ENSP00000251643.4:p.Ser34=
NM_000223.3:c.102T>G NP_000214.1:p.Ser34=
XR_934754.1:n.1500+16225A>C
XR_934754.2:n.2008+16225A>C
NM_000223.4:c.102T>G MANE Select NP_000214.1:p.Ser34=
Search 100 bp 5'
Search 100 bp 3'