Canonical Allele Identifier: CA447449624
Gene: ADAM19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.156995881T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157568873T>C , CM000667.2:g.157568873T>C GRCh38
NC_000005.9:g.156995881T>C , CM000667.1:g.156995881T>C GRCh37
NC_000005.8:g.156928459T>C NCBI36
NG_046960.1:g.11951A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000257527.9:c.180+2022A>G MANE Select ENSP00000257527.5:n.180+2022A>G
ENST00000257527.8:c.180+2022A>G ENSP00000257527.4:n.180+2022A>G
ENST00000517905.1:c.180+2022A>G ENSP00000428654.1:n.180+2022A>G
ENST00000517951.5:c.180+2022A>G ENSP00000428376.1:n.180+2022A>G
NM_033274.4:c.180+2022A>G NP_150377.1:n.180+2022A>G
XM_005266003.2:c.180+2022A>G XP_005266060.1:n.180+2022A>G
NM_033274.5:c.180+2022A>G MANE Select NP_150377.1:n.180+2022A>G
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