Canonical Allele Identifier: CA165821479

Gene: KCND2

Linked Data

• dbSNP Id: rs550090069
• gnomAD v3: 7-120665178-T-C
• gnomAD v4: 7-120665178-T-C
• MyVariant Identifiers: chr7:g.120305232T>C (hg19) ; chr7:g.120665178T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120665178T>C , CM000669.2:g.120665178T>C	GRCh38
NC_000007.13:g.120305232T>C , CM000669.1:g.120305232T>C	GRCh37
NC_000007.12:g.120092468T>C	NCBI36
NG_034230.1:g.396511T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331113.9:c.1116-67725T>C MANE Select	ENSP00000333496.4:n.1116-67725T>C
ENST00000331113.8:c.1116-67725T>C	ENSP00000333496.4:n.1116-67725T>C
NM_012281.2:c.1116-67725T>C	NP_036413.1:n.1116-67725T>C
NM_012281.3:c.1116-67725T>C MANE Select	NP_036413.1:n.1116-67725T>C