Canonical Allele Identifier: CA165821470
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs975837230
gnomAD v2: 7-120305123-A-G
gnomAD v3: 7-120665069-A-G
gnomAD v4: 7-120665069-A-G
MyVariant Identifiers: chr7:g.120305123A>G (hg19) chr7:g.120665069A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665069A>G , CM000669.2:g.120665069A>G GRCh38
NC_000007.13:g.120305123A>G , CM000669.1:g.120305123A>G GRCh37
NC_000007.12:g.120092359A>G NCBI36
NG_034230.1:g.396402A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67834A>G MANE Select ENSP00000333496.4:n.1116-67834A>G
ENST00000331113.8:c.1116-67834A>G ENSP00000333496.4:n.1116-67834A>G
NM_012281.2:c.1116-67834A>G NP_036413.1:n.1116-67834A>G
NM_012281.3:c.1116-67834A>G MANE Select NP_036413.1:n.1116-67834A>G
Search 100 bp 5'
Search 100 bp 3'