Canonical Allele Identifier: CA577561152
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs749158661
gnomAD v2: 7-120304996-C-G
gnomAD v3: 7-120664942-C-G
gnomAD v4: 7-120664942-C-G
MyVariant Identifiers: chr7:g.120304996C>G (hg19) chr7:g.120664942C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120664942C>G , CM000669.2:g.120664942C>G GRCh38
NC_000007.13:g.120304996C>G , CM000669.1:g.120304996C>G GRCh37
NC_000007.12:g.120092232C>G NCBI36
NG_034230.1:g.396275C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67961C>G MANE Select ENSP00000333496.4:n.1116-67961C>G
ENST00000331113.8:c.1116-67961C>G ENSP00000333496.4:n.1116-67961C>G
NM_012281.2:c.1116-67961C>G NP_036413.1:n.1116-67961C>G
NM_012281.3:c.1116-67961C>G MANE Select NP_036413.1:n.1116-67961C>G
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