Canonical Allele Identifier: CA2251974132
Gene: KCNJ12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.21380994C= , CM000679.2:g.21380994C= GRCh38
NC_000017.10:g.21284306C= , CM000679.1:g.21284306C= GRCh37
NC_000017.9:g.21224899C= NCBI36
NG_042809.1:g.9608C=

Transcript Alleles

HGVS Amino-acid change
ENST00000583088.6:c.-179+4081C= MANE Select ENSP00000463778.1:n.-179+4081C=
ENST00000583088.5:c.-179+4081C= ENSP00000463778.1:n.-179+4081C=
NM_021012.4:c.-179+4081C= NP_066292.2:n.-179+4081C=
XM_005256625.3:c.-179+3668C= XP_005256682.1:n.-179+3668C=
XM_005256625.5:c.-179+3668C= XP_005256682.1:n.-179+3668C=
NM_021012.5:c.-179+4081C= MANE Select NP_066292.2:n.-179+4081C=
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