Canonical Allele Identifier: CA93291779
Gene: FAM184B HGNC NCBI

Linked Data

dbSNP Id: rs564563690
gnomAD v3: 4-17681167-T-C
gnomAD v4: 4-17681167-T-C
MyVariant Identifiers: chr4:g.17682790T>C (hg19) chr4:g.17681167T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681167T>C , CM000666.2:g.17681167T>C GRCh38
NC_000004.11:g.17682790T>C , CM000666.1:g.17682790T>C GRCh37
NC_000004.10:g.17291888T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265018.4:c.1596+7257A>G MANE Select ENSP00000265018.3:n.1596+7257A>G
ENST00000265018.3:c.1596+7257A>G ENSP00000265018.3:n.1596+7257A>G
NM_015688.1:c.1596+7257A>G NP_056503.1:n.1596+7257A>G
XM_011513834.1:c.1596+7257A>G XP_011512136.1:n.1596+7257A>G
NM_015688.2:c.1596+7257A>G MANE Select NP_056503.1:n.1596+7257A>G
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