Canonical Allele Identifier: CA32979482
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs996936028
MyVariant Identifiers: chr1:g.172633260T>A (hg19) chr1:g.172664120T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172664120T>A , CM000663.2:g.172664120T>A GRCh38
NC_000001.10:g.172633260T>A , CM000663.1:g.172633260T>A GRCh37
NC_000001.9:g.170899883T>A NCBI36
NG_007269.1:g.10076T>A , LRG_58:g.10076T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.395-214T>A MANE Select ENSP00000356694.2:n.395-214T>A
ENST00000340030.4:c.349-214T>A ENSP00000344739.3:n.349-214T>A
ENST00000367721.2:c.395-214T>A ENSP00000356694.2:n.395-214T>A
NM_000639.2:c.395-214T>A NP_000630.1:n.395-214T>A
NM_001302746.1:c.349-214T>A NP_001289675.1:n.349-214T>A
NM_000639.3:c.395-214T>A MANE Select NP_000630.1:n.395-214T>A
NM_001302746.2:c.349-214T>A NP_001289675.1:n.349-214T>A
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