Canonical Allele Identifier: CA130182493
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs57815709
gnomAD v2: 5-156970160-G-T
gnomAD v3: 5-157543152-G-T
gnomAD v4: 5-157543152-G-T
MyVariant Identifiers: chr5:g.156970160G>T (hg19) chr5:g.157543152G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157543152G>T , CM000667.2:g.157543152G>T GRCh38
NC_000005.9:g.156970160G>T , CM000667.1:g.156970160G>T GRCh37
NC_000005.8:g.156902738G>T NCBI36
NG_046960.1:g.37672C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.252-5161C>A MANE Select ENSP00000257527.5:n.252-5161C>A
ENST00000257527.8:c.252-5161C>A ENSP00000257527.4:n.252-5161C>A
ENST00000517905.1:c.252-5161C>A ENSP00000428654.1:n.252-5161C>A
ENST00000517951.5:c.252-5161C>A ENSP00000428376.1:n.252-5161C>A
NM_033274.4:c.252-5161C>A NP_150377.1:n.252-5161C>A
XM_005266003.2:c.252-5161C>A XP_005266060.1:n.252-5161C>A
NM_033274.5:c.252-5161C>A MANE Select NP_150377.1:n.252-5161C>A
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