Canonical Allele Identifier: CA256721875
Gene: NALF1 HGNC NCBI

Linked Data

dbSNP Id: rs16969868
gnomAD v2: 13-107871712-G-C
gnomAD v3: 13-107219364-G-C
gnomAD v4: 13-107219364-G-C
MyVariant Identifiers: chr13:g.107871712G>C (hg19) chr13:g.107219364G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.107219364G>C , CM000675.2:g.107219364G>C GRCh38
NC_000013.10:g.107871712G>C , CM000675.1:g.107871712G>C GRCh37
NC_000013.9:g.106669713G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375915.4:c.916-8609C>G MANE Select ENSP00000365080.1:n.916-8609C>G
ENST00000375915.3:c.916-8609C>G ENSP00000365080.1:n.916-8609C>G
NM_001080396.2:c.916-8609C>G NP_001073865.1:n.916-8609C>G
XM_011521109.1:c.916-8609C>G XP_011519411.1:n.916-8609C>G
XM_011521109.3:c.916-8609C>G XP_011519411.1:n.916-8609C>G
NM_001080396.3:c.916-8609C>G MANE Select NP_001073865.1:n.916-8609C>G
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