Canonical Allele Identifier: CA2682265789
Gene:

Linked Data

gnomAD v4: 7-30911553-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911553T>G , CM000669.2:g.30911553T>G GRCh38
NC_000007.13:g.30951168T>G , CM000669.1:g.30951168T>G GRCh37
NC_000007.12:g.30917693T>G NCBI36
NG_007475.2:g.63160T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-440T>G