Canonical Allele Identifier: CA769419140

Gene: CALM2

Linked Data

• dbSNP Id: rs1401617957
• gnomAD v3: 2-47162425-A-G
• gnomAD v4: 2-47162425-A-G
• MyVariant Identifiers: chr2:g.47389564A>G (hg19) ; chr2:g.47162425A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47162425A>G , CM000664.2:g.47162425A>G	GRCh38
NC_000002.11:g.47389564A>G , CM000664.1:g.47389564A>G	GRCh37
NC_000002.10:g.47243068A>G	NCBI36
NG_042065.1:g.19512T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272298.12:c.179-33T>C MANE Select	ENSP00000272298.7:n.179-33T>C
ENST00000456319.6:c.71-33T>C	ENSP00000411440.2:n.71-33T>C
ENST00000652974.1:c.*163-33T>C	ENSP00000499369.1:n.*163-33T>C
ENST00000655450.1:c.71-33T>C	ENSP00000499266.1:n.71-33T>C
ENST00000655728.1:c.71-33T>C	ENSP00000499656.1:n.71-33T>C
ENST00000656538.1:c.71-33T>C	ENSP00000499357.1:n.71-33T>C
ENST00000668667.1:c.71-33T>C	ENSP00000499706.1:n.71-33T>C
ENST00000670593.1:n.1084-33T>C
ENST00000272298.11:c.179-33T>C	ENSP00000272298.7:n.179-33T>C
ENST00000409563.5:c.320-33T>C	ENSP00000387065.1:n.320-33T>C
ENST00000422269.1:c.102+8309T>C
ENST00000432899.5:c.178+94T>C	ENSP00000406112.1:n.178+94T>C
ENST00000456319.5:c.293-33T>C	ENSP00000411440.1:n.293-33T>C
ENST00000460218.5:n.3619-33T>C
ENST00000482532.5:n.1446-33T>C
ENST00000484408.5:n.440-33T>C
ENST00000489742.1:n.416-33T>C
ENST00000628793.2:c.165+107T>C	ENSP00000486952.1:n.165+107T>C
NM_001305624.1:c.323-33T>C	NP_001292553.1:n.323-33T>C
NM_001305625.1:c.71-33T>C	NP_001292554.1:n.71-33T>C
NM_001305626.1:c.71-33T>C	NP_001292555.1:n.71-33T>C
NM_001743.4:c.179-33T>C	NP_001734.1:n.179-33T>C
NM_001743.5:c.179-33T>C	NP_001734.1:n.179-33T>C
NM_001743.6:c.179-33T>C MANE Select	NP_001734.1:n.179-33T>C
NM_001305625.2:c.71-33T>C	NP_001292554.1:n.71-33T>C