Canonical Allele Identifier: CA522177789
Gene: FABP3 HGNC NCBI

Linked Data

dbSNP Id: rs1331974767
gnomAD v2: 1-31845971-G-A
gnomAD v3: 1-31373124-G-A
gnomAD v4: 1-31373124-G-A
MyVariant Identifiers: chr1:g.31845971G>A (hg19) chr1:g.31373124G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.31373124G>A , CM000663.2:g.31373124G>A GRCh38
NC_000001.10:g.31845971G>A , CM000663.1:g.31845971G>A GRCh37
NC_000001.9:g.31618558G>A NCBI36
NG_047049.1:g.5160C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000482018.1:c.-27-83C>T ENSP00000473982.1:n.-27-83C>T
XM_011541007.1:c.-110C>T XP_011539309.1:n.-110C>T
NM_001320996.1:c.-110C>T NP_001307925.1:n.-110C>T
NM_004102.4:c.-110C>T NP_004093.1:n.-110C>T
XM_011541007.3:c.-110C>T XP_011539309.1:n.-110C>T
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