Canonical Allele Identifier: CA726977340
Gene: KCNJ12 HGNC NCBI

Linked Data

dbSNP Id: rs1166484496
MyVariant Identifiers: chr17:g.21380949C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.21380949C>T , CM000679.2:g.21380949C>T GRCh38
NC_000017.10:g.21284261C>T , CM000679.1:g.21284261C>T GRCh37
NC_000017.9:g.21224854C>T NCBI36
NG_042809.1:g.9563C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000583088.6:c.-179+4036C>T MANE Select ENSP00000463778.1:n.-179+4036C>T
ENST00000583088.5:c.-179+4036C>T ENSP00000463778.1:n.-179+4036C>T
NM_021012.4:c.-179+4036C>T NP_066292.2:n.-179+4036C>T
XM_005256625.3:c.-179+3623C>T XP_005256682.1:n.-179+3623C>T
XM_005256625.5:c.-179+3623C>T XP_005256682.1:n.-179+3623C>T
NM_021012.5:c.-179+4036C>T MANE Select NP_066292.2:n.-179+4036C>T
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