Canonical Allele Identifier: CA93291748
Gene: FAM184B HGNC NCBI

Linked Data

dbSNP Id: rs1051492321
MyVariant Identifiers: chr4:g.17682690T>G (hg19) chr4:g.17681067T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681067T>G , CM000666.2:g.17681067T>G GRCh38
NC_000004.11:g.17682690T>G , CM000666.1:g.17682690T>G GRCh37
NC_000004.10:g.17291788T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265018.4:c.1596+7357A>C MANE Select ENSP00000265018.3:n.1596+7357A>C
ENST00000265018.3:c.1596+7357A>C ENSP00000265018.3:n.1596+7357A>C
NM_015688.1:c.1596+7357A>C NP_056503.1:n.1596+7357A>C
XM_011513834.1:c.1596+7357A>C XP_011512136.1:n.1596+7357A>C
NM_015688.2:c.1596+7357A>C MANE Select NP_056503.1:n.1596+7357A>C
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