Canonical Allele Identifier: CA156094595

Gene:

Linked Data

• dbSNP Id: rs559649118
• gnomAD v3: 7-30897645-C-T
• gnomAD v4: 7-30897645-C-T
• MyVariant Identifiers: chr7:g.30937260C>T (hg19) ; chr7:g.30897645C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30897645C>T , CM000669.2:g.30897645C>T	GRCh38
NC_000007.13:g.30937260C>T , CM000669.1:g.30937260C>T	GRCh37
NC_000007.12:g.30903785C>T	NCBI36
NG_007475.2:g.49252C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000509504.2:c.622-14348C>T