Canonical Allele Identifier: CA2251974131
Gene: KCNJ12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.21380992G= , CM000679.2:g.21380992G= GRCh38
NC_000017.10:g.21284304G= , CM000679.1:g.21284304G= GRCh37
NC_000017.9:g.21224897G= NCBI36
NG_042809.1:g.9606G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000583088.6:c.-179+4079G= MANE Select ENSP00000463778.1:n.-179+4079G=
ENST00000583088.5:c.-179+4079G= ENSP00000463778.1:n.-179+4079G=
NM_021012.4:c.-179+4079G= NP_066292.2:n.-179+4079G=
XM_005256625.3:c.-179+3666G= XP_005256682.1:n.-179+3666G=
XM_005256625.5:c.-179+3666G= XP_005256682.1:n.-179+3666G=
NM_021012.5:c.-179+4079G= MANE Select NP_066292.2:n.-179+4079G=