Canonical Allele Identifier: CA20151470
Gene: FABP3 HGNC NCBI

Linked Data

dbSNP Id: rs1051168479
MyVariant Identifiers: chr1:g.31373195T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.31373195T>G , CM000663.2:g.31373195T>G GRCh38
NC_000001.10:g.31846042T>G , CM000663.1:g.31846042T>G GRCh37
NC_000001.9:g.31618629T>G NCBI36
NG_047049.1:g.5089A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000482018.1:c.-27-154A>C ENSP00000473982.1:n.-27-154A>C
XM_011541007.1:c.-181A>C XP_011539309.1:n.-181A>C
NM_001320996.1:c.-181A>C NP_001307925.1:n.-181A>C
NM_004102.4:c.-181A>C NP_004093.1:n.-181A>C
XM_011541007.3:c.-181A>C XP_011539309.1:n.-181A>C
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