Canonical Allele Identifier: CA276896052

Gene: MEFV

Linked Data

• dbSNP Id: rs746467645
• gnomAD v2: 16-3294398-T-C
• gnomAD v3: 16-3244398-T-C
• gnomAD v4: 16-3244398-T-C
• MyVariant Identifiers: chr16:g.3294398T>C (hg19) ; chr16:g.3244398T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3244398T>C , CM000678.2:g.3244398T>C	GRCh38
NC_000016.9:g.3294398T>C , CM000678.1:g.3294398T>C	GRCh37
NC_000016.8:g.3234399T>C	NCBI36
NG_007871.1:g.17230A>G , LRG_190:g.17230A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.847+75A>G
ENST00000219596.6:c.1726+75A>G MANE Select	ENSP00000219596.1:n.1726+75A>G
ENST00000219596.5:c.1726+75A>G	ENSP00000219596.1:n.1726+75A>G
ENST00000339854.8:c.1186+75A>G	ENSP00000339639.4:n.1186+75A>G
ENST00000536379.5:c.1093+75A>G	ENSP00000445079.1:n.1093+75A>G
ENST00000536980.5:c.1093+75A>G	ENSP00000444178.1:n.1093+75A>G
ENST00000537682.5:c.1726+75A>G	ENSP00000438611.1:n.1726+75A>G
ENST00000538326.5:c.*351+75A>G	ENSP00000437486.1:n.*351+75A>G
ENST00000539145.5:c.647+75A>G	ENSP00000444471.1:n.647+75A>G
ENST00000541159.5:c.1093+75A>G	ENSP00000438711.1:n.1093+75A>G
ENST00000542898.5:c.1819+75A>G	ENSP00000444615.1:n.1819+75A>G
ENST00000570511.5:c.1165-506A>G	ENSP00000458312.1:n.1165-506A>G
ENST00000572244.5:c.416+75A>G	ENSP00000461186.1:n.416+75A>G
ENST00000574583.5:c.532-506A>G	ENSP00000460269.1:n.532-506A>G
ENST00000576315.5:c.532-112A>G	ENSP00000460551.1:n.532-112A>G
ENST00000621655.1:c.1093+75A>G	ENSP00000481436.1:n.1093+75A>G
NM_000243.2:c.1726+75A>G , LRG_190t1:c.1726+75A>G	NP_000234.1:n.1726+75A>G
NM_001198536.1:c.1093+75A>G	NP_001185465.1:n.1093+75A>G
XM_017023236.2:c.1723+75A>G	XP_016878725.1:n.1723+75A>G
XR_001751903.1:n.1915+75A>G
NM_000243.3:c.1726+75A>G MANE Select	NP_000234.1:n.1726+75A>G
NM_001198536.2:c.1093+75A>G	NP_001185465.2:n.1093+75A>G