Canonical Allele Identifier: CA791396720
Gene: FAM184B HGNC NCBI

Linked Data

dbSNP Id: rs1387379496
gnomAD v3: 4-17681239-T-A
gnomAD v4: 4-17681239-T-A
MyVariant Identifiers: chr4:g.17682862T>A (hg19) chr4:g.17681239T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681239T>A , CM000666.2:g.17681239T>A GRCh38
NC_000004.11:g.17682862T>A , CM000666.1:g.17682862T>A GRCh37
NC_000004.10:g.17291960T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265018.4:c.1596+7185A>T MANE Select ENSP00000265018.3:n.1596+7185A>T
ENST00000265018.3:c.1596+7185A>T ENSP00000265018.3:n.1596+7185A>T
NM_015688.1:c.1596+7185A>T NP_056503.1:n.1596+7185A>T
XM_011513834.1:c.1596+7185A>T XP_011512136.1:n.1596+7185A>T
NM_015688.2:c.1596+7185A>T MANE Select NP_056503.1:n.1596+7185A>T
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