Canonical Allele Identifier: CA1793441483

Gene: KCNB2

Linked Data

• dbSNP Id: rs1805515714

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866225T>C , CM000670.2:g.72866225T>C	GRCh38
NC_000008.10:g.73778460T>C , CM000670.1:g.73778460T>C	GRCh37
NC_000008.9:g.73941014T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523207.2:c.580-69710T>C MANE Select	ENSP00000430846.1:n.580-69710T>C
ENST00000523207.1:c.580-69710T>C	ENSP00000430846.1:n.580-69710T>C
NM_004770.2:c.580-69710T>C	NP_004761.2:n.580-69710T>C
XM_017013981.1:c.-157+2521T>C	XP_016869470.1:n.-157+2521T>C
XR_001745620.1:n.1141-69710T>C
XR_001745621.1:n.1141-69710T>C
NM_004770.3:c.580-69710T>C MANE Select	NP_004761.2:n.580-69710T>C