Canonical Allele Identifier: CA394485179

Gene: MEFV

Linked Data

• dbSNP Id: rs1277277711
• gnomAD v2: 16-3293271-T-C
• gnomAD v4: 16-3243271-T-C
• MyVariant Identifiers: chr16:g.3293271T>C (hg19) ; chr16:g.3243271T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243271T>C , CM000678.2:g.3243271T>C	GRCh38
NC_000016.9:g.3293271T>C , CM000678.1:g.3293271T>C	GRCh37
NC_000016.8:g.3233272T>C	NCBI36
NG_007871.1:g.18357A>G , LRG_190:g.18357A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1337A>G
ENST00000219596.6:c.2216A>G MANE Select	ENSP00000219596.1:p.His739Arg
ENST00000219596.5:c.2216A>G	ENSP00000219596.1:p.His739Arg
ENST00000339854.8:c.1676A>G	ENSP00000339639.4:p.His559Arg
ENST00000536379.5:c.1583A>G	ENSP00000445079.1:p.His528Arg
ENST00000536980.5:c.*492A>G	ENSP00000444178.1:n.*492A>G
ENST00000537682.5:c.*492A>G	ENSP00000438611.1:n.*492A>G
ENST00000538326.5:c.*841A>G	ENSP00000437486.1:n.*841A>G
ENST00000539145.5:c.1137A>G	ENSP00000444471.1:n.1137A>G
ENST00000541159.5:c.1758A>G	ENSP00000438711.1:n.1758A>G
ENST00000542898.5:c.*492A>G	ENSP00000444615.1:n.*492A>G
ENST00000570511.5:c.1621A>G	ENSP00000458312.1:n.1621A>G
ENST00000572244.5:c.906A>G	ENSP00000461186.1:n.906A>G
ENST00000574583.5:c.988A>G	ENSP00000460269.1:n.988A>G
ENST00000576315.5:c.1021A>G	ENSP00000460551.1:n.1021A>G
ENST00000621655.1:c.1753A>G	ENSP00000481436.1:n.1753A>G
NM_000243.2:c.2216A>G , LRG_190t1:c.2216A>G	NP_000234.1:p.His739Arg
NM_001198536.1:c.*420A>G	NP_001185465.1:n.*420A>G
XM_017023236.2:c.2213A>G	XP_016878725.1:p.His738Arg
NM_000243.3:c.2216A>G MANE Select	NP_000234.1:p.His739Arg
NM_001198536.2:c.*420A>G	NP_001185465.2:n.*420A>G