Canonical Allele Identifier: CA791396661
Gene: FAM184B HGNC NCBI

Linked Data

dbSNP Id: rs991321569
MyVariant Identifiers: chr4:g.17682644T>C (hg19) chr4:g.17681021T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681021T>C , CM000666.2:g.17681021T>C GRCh38
NC_000004.11:g.17682644T>C , CM000666.1:g.17682644T>C GRCh37
NC_000004.10:g.17291742T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265018.4:c.1596+7403A>G MANE Select ENSP00000265018.3:n.1596+7403A>G
ENST00000265018.3:c.1596+7403A>G ENSP00000265018.3:n.1596+7403A>G
NM_015688.1:c.1596+7403A>G NP_056503.1:n.1596+7403A>G
XM_011513834.1:c.1596+7403A>G XP_011512136.1:n.1596+7403A>G
NM_015688.2:c.1596+7403A>G MANE Select NP_056503.1:n.1596+7403A>G
Search 100 bp 5'
Search 100 bp 3'