Canonical Allele Identifier: CA2838198392
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161611379A>T , CM000663.2:g.161611379A>T GRCh38
NC_000001.10:g.161581169A>T , CM000663.1:g.161581169A>T GRCh37
NC_000001.9:g.159847793A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.40+19676T>A ENSP00000514363.1:n.40+19676T>A
ENST00000699403.1:c.61+18989T>A ENSP00000514364.1:n.61+18989T>A
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