Canonical Allele Identifier: CA2598416709
Gene:

Linked Data

dbSNP Id: rs2100525024
gnomAD v3: 1-56385038-T-G
gnomAD v4: 1-56385038-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56385038T>G , CM000663.2:g.56385038T>G GRCh38
NC_000001.10:g.56850710T>G , CM000663.1:g.56850710T>G GRCh37
NC_000001.9:g.56623298T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.759+93848A>C ENSP00000493138.1:n.759+93848A>C
ENST00000641346.1:c.366+15056A>C
ENST00000641415.1:c.192+98225A>C
ENST00000641494.1:c.378+98225A>C
ENST00000642129.1:c.768+98225A>C