Canonical Allele Identifier: CA1738824444
Gene: KCND2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120664951A= , CM000669.2:g.120664951A= GRCh38
NC_000007.13:g.120305005A= , CM000669.1:g.120305005A= GRCh37
NC_000007.12:g.120092241A= NCBI36
NG_034230.1:g.396284A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67952A= MANE Select ENSP00000333496.4:n.1116-67952A=
ENST00000331113.8:c.1116-67952A= ENSP00000333496.4:n.1116-67952A=
NM_012281.2:c.1116-67952A= NP_036413.1:n.1116-67952A=
NM_012281.3:c.1116-67952A= MANE Select NP_036413.1:n.1116-67952A=