Canonical Allele Identifier: CA734956927
Gene: FABP3 HGNC NCBI

Linked Data

dbSNP Id: rs1178289282
gnomAD v3: 1-31373204-C-T
gnomAD v4: 1-31373204-C-T
MyVariant Identifiers: chr1:g.31846051C>T (hg19) chr1:g.31373204C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.31373204C>T , CM000663.2:g.31373204C>T GRCh38
NC_000001.10:g.31846051C>T , CM000663.1:g.31846051C>T GRCh37
NC_000001.9:g.31618638C>T NCBI36
NG_047049.1:g.5080G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000482018.1:c.-27-163G>A ENSP00000473982.1:n.-27-163G>A
XM_011541007.1:c.-190G>A XP_011539309.1:n.-190G>A
NM_001320996.1:c.-190G>A NP_001307925.1:n.-190G>A
NM_004102.4:c.-190G>A NP_004093.1:n.-190G>A
XM_011541007.3:c.-190G>A XP_011539309.1:n.-190G>A
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