Canonical Allele Identifier: CA1738824754
Gene: KCND2 HGNC NCBI

Linked Data

dbSNP Id: rs1791910187
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120665191A>T , CM000669.2:g.120665191A>T GRCh38
NC_000007.13:g.120305245A>T , CM000669.1:g.120305245A>T GRCh37
NC_000007.12:g.120092481A>T NCBI36
NG_034230.1:g.396524A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331113.9:c.1116-67712A>T MANE Select ENSP00000333496.4:n.1116-67712A>T
ENST00000331113.8:c.1116-67712A>T ENSP00000333496.4:n.1116-67712A>T
NM_012281.2:c.1116-67712A>T NP_036413.1:n.1116-67712A>T
NM_012281.3:c.1116-67712A>T MANE Select NP_036413.1:n.1116-67712A>T
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