Canonical Allele Identifier: CA370151138
Gene: SHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.155604556C>G (hg19) chr7:g.155811862C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155811862C>G , CM000669.2:g.155811862C>G GRCh38
NC_000007.13:g.155604556C>G , CM000669.1:g.155604556C>G GRCh37
NC_000007.12:g.155297317C>G NCBI36
NG_007504.2:g.5412G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297261.7:c.261G>C MANE Select ENSP00000297261.2:p.Lys87Asn
ENST00000297261.6:c.261G>C ENSP00000297261.2:p.Lys87Asn
NM_000193.2:c.261G>C NP_000184.1:p.Lys87Asn
NM_000193.3:c.261G>C NP_000184.1:p.Lys87Asn
NM_000193.4:c.261G>C MANE Select NP_000184.1:p.Lys87Asn
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