Canonical Allele Identifier: CA720023963

Gene: MEFV

Linked Data

• dbSNP Id: rs1397413313
• MyVariant Identifiers: chr16:g.3293002A>G (hg19) ; chr16:g.3243002A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3243002A>G , CM000678.2:g.3243002A>G	GRCh38
NC_000016.9:g.3293002A>G , CM000678.1:g.3293002A>G	GRCh37
NC_000016.8:g.3233003A>G	NCBI36
NG_007871.1:g.18626T>C , LRG_190:g.18626T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1606T>C
ENST00000219596.6:c.*139T>C MANE Select	ENSP00000219596.1:n.*139T>C
ENST00000219596.5:c.*139T>C	ENSP00000219596.1:n.*139T>C
ENST00000339854.8:c.*139T>C	ENSP00000339639.4:n.*139T>C
ENST00000536980.5:c.*761T>C	ENSP00000444178.1:n.*761T>C
ENST00000537682.5:c.*761T>C	ENSP00000438611.1:n.*761T>C
ENST00000538326.5:c.*1110T>C	ENSP00000437486.1:n.*1110T>C
ENST00000542898.5:c.*761T>C	ENSP00000444615.1:n.*761T>C
NM_000243.2:c.*139T>C , LRG_190t1:c.*139T>C	NP_000234.1:n.*139T>C
NM_001198536.1:c.*689T>C	NP_001185465.1:n.*689T>C
NM_000243.3:c.*139T>C MANE Select	NP_000234.1:n.*139T>C
NM_001198536.2:c.*689T>C	NP_001185465.2:n.*689T>C