Canonical Allele Identifier: CA278262944
Gene: LITAF HGNC NCBI

Linked Data

dbSNP Id: rs762434936
gnomAD v2: 16-11691659-C-T
gnomAD v3: 16-11597803-C-T
gnomAD v4: 16-11597803-C-T
MyVariant Identifiers: chr16:g.11691659C>T (hg19) chr16:g.11597803C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11597803C>T , CM000678.2:g.11597803C>T GRCh38
NC_000016.9:g.11691659C>T , CM000678.1:g.11691659C>T GRCh37
NC_000016.8:g.11599160C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000571627.5:c.-6+585G>A ENSP00000460743.1:n.-6+585G>A
ENST00000574848.5:c.85+35730G>A ENSP00000459898.1:n.85+35730G>A
ENST00000576036.5:c.-6+31320G>A ENSP00000461667.1:n.-6+31320G>A
ENST00000576334.1:c.85+35730G>A ENSP00000458538.1:n.85+35730G>A
XM_011522754.1:c.85+35730G>A XP_011521056.1:n.85+35730G>A
XM_011522754.3:c.85+35730G>A XP_011521056.1:n.85+35730G>A
XM_017023896.1:c.-6+31320G>A XP_016879385.1:n.-6+31320G>A
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