Canonical Allele Identifier: CA169426492
Gene: SHH HGNC NCBI

Linked Data

dbSNP Id: rs894022121
gnomAD v3: 7-155812159-G-T
gnomAD v4: 7-155812159-G-T
MyVariant Identifiers: chr7:g.155604853G>T (hg19) chr7:g.155812159G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155812159G>T , CM000669.2:g.155812159G>T GRCh38
NC_000007.13:g.155604853G>T , CM000669.1:g.155604853G>T GRCh37
NC_000007.12:g.155297614G>T NCBI36
NG_007504.2:g.5115C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297261.7:c.-37C>A MANE Select ENSP00000297261.2:n.-37C>A
ENST00000297261.6:c.-37C>A ENSP00000297261.2:n.-37C>A
NM_000193.2:c.-37C>A NP_000184.1:n.-37C>A
NM_000193.3:c.-37C>A NP_000184.1:n.-37C>A
NM_000193.4:c.-37C>A MANE Select NP_000184.1:n.-37C>A
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