Canonical Allele Identifier: CA1738824734

Gene: KCND2

Linked Data

• dbSNP Id: rs1791909965

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120665165A>C , CM000669.2:g.120665165A>C	GRCh38
NC_000007.13:g.120305219A>C , CM000669.1:g.120305219A>C	GRCh37
NC_000007.12:g.120092455A>C	NCBI36
NG_034230.1:g.396498A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331113.9:c.1116-67738A>C MANE Select	ENSP00000333496.4:n.1116-67738A>C
ENST00000331113.8:c.1116-67738A>C	ENSP00000333496.4:n.1116-67738A>C
NM_012281.2:c.1116-67738A>C	NP_036413.1:n.1116-67738A>C
NM_012281.3:c.1116-67738A>C MANE Select	NP_036413.1:n.1116-67738A>C