Canonical Allele Identifier: CA31364648
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs375270171
gnomAD v2: 1-159272146-A-G
gnomAD v3: 1-159302356-A-G
gnomAD v4: 1-159302356-A-G
MyVariant Identifiers: chr1:g.159272146A>G (hg19) chr1:g.159302356A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302356A>G , CM000663.2:g.159302356A>G GRCh38
NC_000001.10:g.159272146A>G , CM000663.1:g.159272146A>G GRCh37
NC_000001.9:g.157538770A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693622.1:c.-9A>G MANE Select ENSP00000509626.1:n.-9A>G
ENST00000368114.1:c.-9A>G ENSP00000357096.1:n.-9A>G
ENST00000368115.5:c.-9A>G ENSP00000357097.1:n.-9A>G
NM_002001.3:c.-9A>G NP_001992.1:n.-9A>G
NM_001387280.1:c.-9A>G MANE Select NP_001374209.1:n.-9A>G
NM_001387281.1:c.-9A>G NP_001374210.1:n.-9A>G
NM_001387282.1:c.-9A>G NP_001374211.1:n.-9A>G
NM_002001.4:c.-9A>G NP_001992.1:n.-9A>G
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