Canonical Allele Identifier: CA718049805
Gene: LITAF HGNC NCBI

Linked Data

dbSNP Id: rs1414709845
gnomAD v3: 16-11597935-C-A
gnomAD v4: 16-11597935-C-A
MyVariant Identifiers: chr16:g.11691791C>A (hg19) chr16:g.11597935C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11597935C>A , CM000678.2:g.11597935C>A GRCh38
NC_000016.9:g.11691791C>A , CM000678.1:g.11691791C>A GRCh37
NC_000016.8:g.11599292C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000571627.5:c.-6+453G>T ENSP00000460743.1:n.-6+453G>T
ENST00000574848.5:c.85+35598G>T ENSP00000459898.1:n.85+35598G>T
ENST00000576036.5:c.-6+31188G>T ENSP00000461667.1:n.-6+31188G>T
ENST00000576334.1:c.85+35598G>T ENSP00000458538.1:n.85+35598G>T
XM_011522754.1:c.85+35598G>T XP_011521056.1:n.85+35598G>T
XM_011522754.3:c.85+35598G>T XP_011521056.1:n.85+35598G>T
XM_017023896.1:c.-6+31188G>T XP_016879385.1:n.-6+31188G>T
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