Canonical Allele Identifier: CA522177797
Gene: FABP3 HGNC NCBI

Linked Data

dbSNP Id: rs989080585
gnomAD v2: 1-31846037-G-C
gnomAD v3: 1-31373190-G-C
gnomAD v4: 1-31373190-G-C
MyVariant Identifiers: chr1:g.31846037G>C (hg19) chr1:g.31373190G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.31373190G>C , CM000663.2:g.31373190G>C GRCh38
NC_000001.10:g.31846037G>C , CM000663.1:g.31846037G>C GRCh37
NC_000001.9:g.31618624G>C NCBI36
NG_047049.1:g.5094C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000482018.1:c.-27-149C>G ENSP00000473982.1:n.-27-149C>G
XM_011541007.1:c.-176C>G XP_011539309.1:n.-176C>G
NM_001320996.1:c.-176C>G NP_001307925.1:n.-176C>G
NM_004102.4:c.-176C>G NP_004093.1:n.-176C>G
XM_011541007.3:c.-176C>G XP_011539309.1:n.-176C>G
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