Canonical Allele Identifier: CA734956925
Gene: FABP3 HGNC NCBI

Linked Data

dbSNP Id: rs1051168479
gnomAD v3: 1-31373195-T-C
gnomAD v4: 1-31373195-T-C
MyVariant Identifiers: chr1:g.31846042T>C (hg19) chr1:g.31373195T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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