Canonical Allele Identifier: CA1793441496
Gene: KCNB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866258C= , CM000670.2:g.72866258C= GRCh38
NC_000008.10:g.73778493C= , CM000670.1:g.73778493C= GRCh37
NC_000008.9:g.73941047C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523207.2:c.580-69677C= MANE Select ENSP00000430846.1:n.580-69677C=
ENST00000523207.1:c.580-69677C= ENSP00000430846.1:n.580-69677C=
NM_004770.2:c.580-69677C= NP_004761.2:n.580-69677C=
XM_017013981.1:c.-157+2554C= XP_016869470.1:n.-157+2554C=
XR_001745620.1:n.1141-69677C=
XR_001745621.1:n.1141-69677C=
NM_004770.3:c.580-69677C= MANE Select NP_004761.2:n.580-69677C=