Canonical Allele Identifier: CA2682265787
Gene:

Linked Data

gnomAD v4: 7-30911550-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911550G>T , CM000669.2:g.30911550G>T GRCh38
NC_000007.13:g.30951165G>T , CM000669.1:g.30951165G>T GRCh37
NC_000007.12:g.30917690G>T NCBI36
NG_007475.2:g.63157G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-443G>T