Canonical Allele Identifier: CA2251974125
Gene: KCNJ12 HGNC NCBI

Linked Data

dbSNP Id: rs1904845379
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.21380979T>C , CM000679.2:g.21380979T>C GRCh38
NC_000017.10:g.21284291T>C , CM000679.1:g.21284291T>C GRCh37
NC_000017.9:g.21224884T>C NCBI36
NG_042809.1:g.9593T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000583088.6:c.-179+4066T>C MANE Select ENSP00000463778.1:n.-179+4066T>C
ENST00000583088.5:c.-179+4066T>C ENSP00000463778.1:n.-179+4066T>C
NM_021012.4:c.-179+4066T>C NP_066292.2:n.-179+4066T>C
XM_005256625.3:c.-179+3653T>C XP_005256682.1:n.-179+3653T>C
XM_005256625.5:c.-179+3653T>C XP_005256682.1:n.-179+3653T>C
NM_021012.5:c.-179+4066T>C MANE Select NP_066292.2:n.-179+4066T>C
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