Canonical Allele Identifier: CA155828835
Gene:

Linked Data

dbSNP Id: rs996418838
MyVariant Identifiers: chr7:g.24323242G>C (hg19) chr7:g.24283623G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283623G>C , CM000669.2:g.24283623G>C GRCh38
NC_000007.13:g.24323242G>C , CM000669.1:g.24323242G>C GRCh37
NC_000007.12:g.24289767G>C NCBI36
NG_016148.1:g.4436G>C

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.42-27924C>G XP_016868399.1:n.42-27924C>G
XM_017012911.1:c.42-27924C>G XP_016868400.1:n.42-27924C>G
XR_001745121.1:n.473+35734C>G
XR_001745122.1:n.345-86594C>G
XR_001745123.1:n.473+35734C>G
XR_001745124.1:n.473+35734C>G
XR_001745125.1:n.473+35734C>G
XR_001745126.1:n.473+35734C>G
XR_001745127.1:n.345-27924C>G
XR_001745129.1:n.473+35734C>G
XR_001745130.1:n.473+35734C>G
XR_001745131.1:n.473+35734C>G
XR_001745132.1:n.473+35734C>G
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