Canonical Allele Identifier: CA908188463
Gene:

Linked Data

dbSNP Id: rs1341652052
gnomAD v3: 3-53057137-A-G
gnomAD v4: 3-53057137-A-G
MyVariant Identifiers: chr3:g.53091153A>G (hg19) chr3:g.53057137A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057137A>G , CM000665.2:g.53057137A>G GRCh38
NC_000003.11:g.53091153A>G , CM000665.1:g.53091153A>G GRCh37
NC_000003.10:g.53066193A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9898T>C
ENST00000607283.5:c.465-13883T>C
ENST00000607495.5:c.447+20551T>C
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