Canonical Allele Identifier: CA1441689175
Gene: FAM184B HGNC NCBI

Linked Data

dbSNP Id: rs1716422301
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681042C>A , CM000666.2:g.17681042C>A GRCh38
NC_000004.11:g.17682665C>A , CM000666.1:g.17682665C>A GRCh37
NC_000004.10:g.17291763C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265018.4:c.1596+7382G>T MANE Select ENSP00000265018.3:n.1596+7382G>T
ENST00000265018.3:c.1596+7382G>T ENSP00000265018.3:n.1596+7382G>T
NM_015688.1:c.1596+7382G>T NP_056503.1:n.1596+7382G>T
XM_011513834.1:c.1596+7382G>T XP_011512136.1:n.1596+7382G>T
NM_015688.2:c.1596+7382G>T MANE Select NP_056503.1:n.1596+7382G>T
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