Canonical Allele Identifier: CA1793441487

Gene: KCNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866233_72866235delinsATG , CM000670.2:g.72866233_72866235delinsATG	GRCh38
NC_000008.10:g.73778468_73778470delinsATG , CM000670.1:g.73778468_73778470delinsATG	GRCh37
NC_000008.9:g.73941022_73941024delinsATG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523207.2:c.580-69702_580-69700delinsATG MANE Select	ENSP00000430846.1:n.580-69702_580-69700delinsATG
ENST00000523207.1:c.580-69702_580-69700delinsATG	ENSP00000430846.1:n.580-69702_580-69700delinsATG
NM_004770.2:c.580-69702_580-69700delinsATG	NP_004761.2:n.580-69702_580-69700delinsATG
XM_017013981.1:c.-157+2529_-157+2531delinsATG	XP_016869470.1:n.-157+2529_-157+2531delinsATG
XR_001745620.1:n.1141-69702_1141-69700delinsATG
XR_001745621.1:n.1141-69702_1141-69700delinsATG
NM_004770.3:c.580-69702_580-69700delinsATG MANE Select	NP_004761.2:n.580-69702_580-69700delinsATG