Canonical Allele Identifier: CA1014783648
Gene:

Linked Data

dbSNP Id: rs2085111788
gnomAD v3: 20-2470964-A-G
gnomAD v4: 20-2470964-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470964A>G , CM000682.2:g.2470964A>G GRCh38
NC_000020.10:g.2451610A>G , CM000682.1:g.2451610A>G GRCh37
NC_000020.9:g.2399610A>G NCBI36
NG_042057.1:g.4890T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3206T>C ENSP00000456213.1:n.305-3206T>C