Canonical Allele Identifier: CA278262959
Gene: LITAF HGNC NCBI

Linked Data

dbSNP Id: rs369853186
gnomAD v2: 16-11691665-A-G
gnomAD v3: 16-11597809-A-G
gnomAD v4: 16-11597809-A-G
MyVariant Identifiers: chr16:g.11691665A>G (hg19) chr16:g.11597809A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11597809A>G , CM000678.2:g.11597809A>G GRCh38
NC_000016.9:g.11691665A>G , CM000678.1:g.11691665A>G GRCh37
NC_000016.8:g.11599166A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000571627.5:c.-6+579T>C ENSP00000460743.1:n.-6+579T>C
ENST00000574848.5:c.85+35724T>C ENSP00000459898.1:n.85+35724T>C
ENST00000576036.5:c.-6+31314T>C ENSP00000461667.1:n.-6+31314T>C
ENST00000576334.1:c.85+35724T>C ENSP00000458538.1:n.85+35724T>C
XM_011522754.1:c.85+35724T>C XP_011521056.1:n.85+35724T>C
XM_011522754.3:c.85+35724T>C XP_011521056.1:n.85+35724T>C
XM_017023896.1:c.-6+31314T>C XP_016879385.1:n.-6+31314T>C
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