Canonical Allele Identifier: CA343057060

Gene: FCER1A

Linked Data

• dbSNP Id: rs1394253482
• gnomAD v2: 1-159272155-A-G
• gnomAD v4: 1-159302365-A-G
• MyVariant Identifiers: chr1:g.159272155A>G (hg19) ; chr1:g.159302365A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159302365A>G , CM000663.2:g.159302365A>G	GRCh38
NC_000001.10:g.159272155A>G , CM000663.1:g.159272155A>G	GRCh37
NC_000001.9:g.157538779A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693622.1:c.1A>G MANE Select	ENSP00000509626.1:p.Met1Val
ENST00000368114.1:c.1A>G	ENSP00000357096.1:p.Met1Val
ENST00000368115.5:c.1A>G	ENSP00000357097.1:p.Met1Val
NM_002001.3:c.1A>G	NP_001992.1:p.Met1Val
NM_001387280.1:c.1A>G MANE Select	NP_001374209.1:p.Met1Val
NM_001387281.1:c.1A>G	NP_001374210.1:p.Met1Val
NM_001387282.1:c.1A>G	NP_001374211.1:p.Met1Val
NM_002001.4:c.1A>G	NP_001992.1:p.Met1Val