Canonical Allele Identifier: CA93291786
Gene: FAM184B HGNC NCBI

Linked Data

dbSNP Id: rs546927494
gnomAD v3: 4-17681192-A-T
gnomAD v4: 4-17681192-A-T
MyVariant Identifiers: chr4:g.17682815A>T (hg19) chr4:g.17681192A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681192A>T , CM000666.2:g.17681192A>T GRCh38
NC_000004.11:g.17682815A>T , CM000666.1:g.17682815A>T GRCh37
NC_000004.10:g.17291913A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265018.4:c.1596+7232T>A MANE Select ENSP00000265018.3:n.1596+7232T>A
ENST00000265018.3:c.1596+7232T>A ENSP00000265018.3:n.1596+7232T>A
NM_015688.1:c.1596+7232T>A NP_056503.1:n.1596+7232T>A
XM_011513834.1:c.1596+7232T>A XP_011512136.1:n.1596+7232T>A
NM_015688.2:c.1596+7232T>A MANE Select NP_056503.1:n.1596+7232T>A
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