Canonical Allele Identifier: CA2570708272
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056970G>T , CM000665.2:g.53056970G>T GRCh38
NC_000003.11:g.53090986G>T , CM000665.1:g.53090986G>T GRCh37
NC_000003.10:g.53066026G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9731C>A
ENST00000607283.5:c.465-13716C>A
ENST00000607495.5:c.447+20718C>A
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