Canonical Allele Identifier: CA155828716

Gene:

Linked Data

• dbSNP Id: rs970515572
• gnomAD v2: 7-24322308-T-C
• gnomAD v3: 7-24282689-T-C
• gnomAD v4: 7-24282689-T-C
• MyVariant Identifiers: chr7:g.24322308T>C (hg19) ; chr7:g.24282689T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24282689T>C , CM000669.2:g.24282689T>C	GRCh38
NC_000007.13:g.24322308T>C , CM000669.1:g.24322308T>C	GRCh37
NC_000007.12:g.24288833T>C	NCBI36
NG_016148.1:g.3502T>C

Transcript Alleles

HGVS	Amino-acid change
XM_017012910.1:c.42-26990A>G	XP_016868399.1:n.42-26990A>G
XM_017012911.1:c.42-26990A>G	XP_016868400.1:n.42-26990A>G
XR_001745121.1:n.473+36668A>G
XR_001745122.1:n.345-85660A>G
XR_001745123.1:n.473+36668A>G
XR_001745124.1:n.473+36668A>G
XR_001745125.1:n.473+36668A>G
XR_001745126.1:n.473+36668A>G
XR_001745127.1:n.345-26990A>G
XR_001745129.1:n.473+36668A>G
XR_001745130.1:n.473+36668A>G
XR_001745131.1:n.473+36668A>G
XR_001745132.1:n.473+36668A>G