Canonical Allele Identifier: CA542918786
Gene:

Linked Data

dbSNP Id: rs1419553680
gnomAD v2: 3-53090929-G-A
gnomAD v3: 3-53056913-G-A
gnomAD v4: 3-53056913-G-A
MyVariant Identifiers: chr3:g.53090929G>A (hg19) chr3:g.53056913G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056913G>A , CM000665.2:g.53056913G>A GRCh38
NC_000003.11:g.53090929G>A , CM000665.1:g.53090929G>A GRCh37
NC_000003.10:g.53065969G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9674C>T
ENST00000607283.5:c.465-13659C>T
ENST00000607495.5:c.447+20775C>T
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