Canonical Allele Identifier: CA156094475
Gene:

Linked Data

dbSNP Id: rs74326065
gnomAD v3: 7-30897585-C-G
gnomAD v4: 7-30897585-C-G
MyVariant Identifiers: chr7:g.30897585C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897585C>G , CM000669.2:g.30897585C>G GRCh38
NC_000007.13:g.30937200C>G , CM000669.1:g.30937200C>G GRCh37
NC_000007.12:g.30903725C>G NCBI36
NG_007475.2:g.49192C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14408C>G